Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy
Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy....
Ausführliche Beschreibung
Autor*in: |
Du, Rong [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Anmerkung: |
© Tsinghua University Press 2023 |
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Übergeordnetes Werk: |
Enthalten in: Nano research - [S.l.] : Tsinghua Press, 2008, 16(2023), 12 vom: 13. Okt., Seite 13309-13321 |
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Übergeordnetes Werk: |
volume:16 ; year:2023 ; number:12 ; day:13 ; month:10 ; pages:13309-13321 |
Links: |
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DOI / URN: |
10.1007/s12274-023-6105-0 |
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Katalog-ID: |
SPR054227348 |
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520 | |a Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. | ||
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650 | 4 | |a docetaxel |7 (dpeaa)DE-He213 | |
650 | 4 | |a small interfering RNA (siRNA) delivery |7 (dpeaa)DE-He213 | |
650 | 4 | |a ovarian cancer |7 (dpeaa)DE-He213 | |
700 | 1 | |a You, Qing |4 aut | |
700 | 1 | |a Liu, Jingyi |4 aut | |
700 | 1 | |a Wang, Chen |4 aut | |
700 | 1 | |a Zhu, Ling |4 aut | |
700 | 1 | |a Yang, Yanlian |4 aut | |
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10.1007/s12274-023-6105-0 doi (DE-627)SPR054227348 (SPR)s12274-023-6105-0-e DE-627 ger DE-627 rakwb eng Du, Rong verfasserin aut Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Tsinghua University Press 2023 Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. extracellular vesicles (dpeaa)DE-He213 N (dpeaa)DE-He213 -methyladenosine (m (dpeaa)DE-He213 A) modulators (dpeaa)DE-He213 docetaxel (dpeaa)DE-He213 small interfering RNA (siRNA) delivery (dpeaa)DE-He213 ovarian cancer (dpeaa)DE-He213 You, Qing aut Liu, Jingyi aut Wang, Chen aut Zhu, Ling aut Yang, Yanlian aut Enthalten in Nano research [S.l.] : Tsinghua Press, 2008 16(2023), 12 vom: 13. Okt., Seite 13309-13321 (DE-627)57375361X (DE-600)2442216-2 1998-0000 nnns volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 https://dx.doi.org/10.1007/s12274-023-6105-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 16 2023 12 13 10 13309-13321 |
spelling |
10.1007/s12274-023-6105-0 doi (DE-627)SPR054227348 (SPR)s12274-023-6105-0-e DE-627 ger DE-627 rakwb eng Du, Rong verfasserin aut Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Tsinghua University Press 2023 Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. extracellular vesicles (dpeaa)DE-He213 N (dpeaa)DE-He213 -methyladenosine (m (dpeaa)DE-He213 A) modulators (dpeaa)DE-He213 docetaxel (dpeaa)DE-He213 small interfering RNA (siRNA) delivery (dpeaa)DE-He213 ovarian cancer (dpeaa)DE-He213 You, Qing aut Liu, Jingyi aut Wang, Chen aut Zhu, Ling aut Yang, Yanlian aut Enthalten in Nano research [S.l.] : Tsinghua Press, 2008 16(2023), 12 vom: 13. Okt., Seite 13309-13321 (DE-627)57375361X (DE-600)2442216-2 1998-0000 nnns volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 https://dx.doi.org/10.1007/s12274-023-6105-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 16 2023 12 13 10 13309-13321 |
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10.1007/s12274-023-6105-0 doi (DE-627)SPR054227348 (SPR)s12274-023-6105-0-e DE-627 ger DE-627 rakwb eng Du, Rong verfasserin aut Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Tsinghua University Press 2023 Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. extracellular vesicles (dpeaa)DE-He213 N (dpeaa)DE-He213 -methyladenosine (m (dpeaa)DE-He213 A) modulators (dpeaa)DE-He213 docetaxel (dpeaa)DE-He213 small interfering RNA (siRNA) delivery (dpeaa)DE-He213 ovarian cancer (dpeaa)DE-He213 You, Qing aut Liu, Jingyi aut Wang, Chen aut Zhu, Ling aut Yang, Yanlian aut Enthalten in Nano research [S.l.] : Tsinghua Press, 2008 16(2023), 12 vom: 13. Okt., Seite 13309-13321 (DE-627)57375361X (DE-600)2442216-2 1998-0000 nnns volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 https://dx.doi.org/10.1007/s12274-023-6105-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 16 2023 12 13 10 13309-13321 |
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10.1007/s12274-023-6105-0 doi (DE-627)SPR054227348 (SPR)s12274-023-6105-0-e DE-627 ger DE-627 rakwb eng Du, Rong verfasserin aut Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Tsinghua University Press 2023 Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. extracellular vesicles (dpeaa)DE-He213 N (dpeaa)DE-He213 -methyladenosine (m (dpeaa)DE-He213 A) modulators (dpeaa)DE-He213 docetaxel (dpeaa)DE-He213 small interfering RNA (siRNA) delivery (dpeaa)DE-He213 ovarian cancer (dpeaa)DE-He213 You, Qing aut Liu, Jingyi aut Wang, Chen aut Zhu, Ling aut Yang, Yanlian aut Enthalten in Nano research [S.l.] : Tsinghua Press, 2008 16(2023), 12 vom: 13. Okt., Seite 13309-13321 (DE-627)57375361X (DE-600)2442216-2 1998-0000 nnns volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 https://dx.doi.org/10.1007/s12274-023-6105-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 16 2023 12 13 10 13309-13321 |
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10.1007/s12274-023-6105-0 doi (DE-627)SPR054227348 (SPR)s12274-023-6105-0-e DE-627 ger DE-627 rakwb eng Du, Rong verfasserin aut Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Tsinghua University Press 2023 Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. extracellular vesicles (dpeaa)DE-He213 N (dpeaa)DE-He213 -methyladenosine (m (dpeaa)DE-He213 A) modulators (dpeaa)DE-He213 docetaxel (dpeaa)DE-He213 small interfering RNA (siRNA) delivery (dpeaa)DE-He213 ovarian cancer (dpeaa)DE-He213 You, Qing aut Liu, Jingyi aut Wang, Chen aut Zhu, Ling aut Yang, Yanlian aut Enthalten in Nano research [S.l.] : Tsinghua Press, 2008 16(2023), 12 vom: 13. Okt., Seite 13309-13321 (DE-627)57375361X (DE-600)2442216-2 1998-0000 nnns volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 https://dx.doi.org/10.1007/s12274-023-6105-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 16 2023 12 13 10 13309-13321 |
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Enthalten in Nano research 16(2023), 12 vom: 13. Okt., Seite 13309-13321 volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 |
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Enthalten in Nano research 16(2023), 12 vom: 13. Okt., Seite 13309-13321 volume:16 year:2023 number:12 day:13 month:10 pages:13309-13321 |
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extracellular vesicles N -methyladenosine (m A) modulators docetaxel small interfering RNA (siRNA) delivery ovarian cancer |
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Du, Rong @@aut@@ You, Qing @@aut@@ Liu, Jingyi @@aut@@ Wang, Chen @@aut@@ Zhu, Ling @@aut@@ Yang, Yanlian @@aut@@ |
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2023-10-13T00:00:00Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000naa a22002652 4500</leader><controlfield tag="001">SPR054227348</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20240103064858.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">240103s2023 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s12274-023-6105-0</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR054227348</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s12274-023-6105-0-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Du, Rong</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2023</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Tsinghua University Press 2023</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. 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|
author |
Du, Rong |
spellingShingle |
Du, Rong misc extracellular vesicles misc N misc -methyladenosine (m misc A) modulators misc docetaxel misc small interfering RNA (siRNA) delivery misc ovarian cancer Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy |
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Du, Rong |
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1998-0000 |
topic_title |
Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy extracellular vesicles (dpeaa)DE-He213 N (dpeaa)DE-He213 -methyladenosine (m (dpeaa)DE-He213 A) modulators (dpeaa)DE-He213 docetaxel (dpeaa)DE-He213 small interfering RNA (siRNA) delivery (dpeaa)DE-He213 ovarian cancer (dpeaa)DE-He213 |
topic |
misc extracellular vesicles misc N misc -methyladenosine (m misc A) modulators misc docetaxel misc small interfering RNA (siRNA) delivery misc ovarian cancer |
topic_unstemmed |
misc extracellular vesicles misc N misc -methyladenosine (m misc A) modulators misc docetaxel misc small interfering RNA (siRNA) delivery misc ovarian cancer |
topic_browse |
misc extracellular vesicles misc N misc -methyladenosine (m misc A) modulators misc docetaxel misc small interfering RNA (siRNA) delivery misc ovarian cancer |
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title |
Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy |
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(DE-627)SPR054227348 (SPR)s12274-023-6105-0-e |
title_full |
Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy |
author_sort |
Du, Rong |
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Nano research |
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Du, Rong You, Qing Liu, Jingyi Wang, Chen Zhu, Ling Yang, Yanlian |
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16 |
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Elektronische Aufsätze |
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Du, Rong |
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10.1007/s12274-023-6105-0 |
title_sort |
dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $a reader ythdf1-targeting epigenetic regulation and chemotherapy |
title_auth |
Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy |
abstract |
Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. © Tsinghua University Press 2023 |
abstractGer |
Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. © Tsinghua University Press 2023 |
abstract_unstemmed |
Abstract Chemotherapy remains one of the most prevailing strategies for cancer treatment. However, its treatment effect is hampered by drug resistance, nonspecific tumor targeting, and severe toxic side effects. Combination chemotherapy with synergistic effect has become an attractive tumor therapy. $ N^{6} $-methyladenosine ($ m^{6} $A) regulators determine the fate of $ m^{6} $A-modified transcripts and play vital roles in cancer development and drug resistance. Gene therapy such as small interfering RNA (siRNA) is a promising strategy to reduce the abnormal gene expression of $ m^{6} $A regulators. However, its poor selectivity and high systemic toxicity necessitate the use of delivery vectors to target specific cells and tissues. Here, we constructed a dual-functional targeted nanodrug platform for the synergetic $ m^{6} $A-associated epigenetic regulation and chemotherapy of ovarian cancer. We encapsulated siRNA targeting the $ m^{6} $A reader YT521-B homology (YTH) $ N^{6} $-methyladenosine RNA-binding protein 1 (YTHDF1) and docetaxel (DTX), the first-line chemotherapeutic agent of ovarian cancer, into mesenchymal stem cell-derived small extracellular vesicles (MsEVs). This nanosystem exhibits significant tumor targeting and endo/lysosomal escape of siYTHDF1. It effectively depletes YTHDF1 and suppresses the protein translation of eukaryotic translation initiation factor 3 subunit C (EIF3C) in an $ m^{6} $A-dependent manner. The combination of YTHDF1-targeting epigenetic regulation significantly enhances the anti-tumor effect of DTX and effectively inhibits ovarian cancer progression without causing significant systemic toxicity. This co-delivery nanoplatform offers a promising approach for combinational cancer treatment, showing improved anti-tumor efficacy through the synergistic effects of epigenetic regulation and chemotherapeutic inhibition. © Tsinghua University Press 2023 |
collection_details |
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container_issue |
12 |
title_short |
Dual-functional extracellular vesicles enable synergistic treatment via $ m^{6} $A reader YTHDF1-targeting epigenetic regulation and chemotherapy |
url |
https://dx.doi.org/10.1007/s12274-023-6105-0 |
remote_bool |
true |
author2 |
You, Qing Liu, Jingyi Wang, Chen Zhu, Ling Yang, Yanlian |
author2Str |
You, Qing Liu, Jingyi Wang, Chen Zhu, Ling Yang, Yanlian |
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hochschulschrift_bool |
false |
doi_str |
10.1007/s12274-023-6105-0 |
up_date |
2024-07-04T00:34:29.279Z |
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|
score |
7.401534 |