The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells
Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyo...
Ausführliche Beschreibung
Autor*in: |
Lozupone, Francesco [verfasserIn] Perdicchio, Maurizio [verfasserIn] Brambilla, Daria [verfasserIn] Borghi, Martina [verfasserIn] Meschini, Stefania [verfasserIn] Barca, Stefano [verfasserIn] Marino, Maria Lucia [verfasserIn] Logozzi, Mariantonia [verfasserIn] Federici, Cristina [verfasserIn] Iessi, Elisabetta [verfasserIn] de Milito, Angelo [verfasserIn] Fais, Stefano [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2009 |
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Schlagwörter: |
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Anmerkung: |
© European Molecular Biology Organization 2009 |
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Übergeordnetes Werk: |
Enthalten in: EMBO Reports - Nature Publishing Group UK, 2023, 10(2009), 12 vom: 06. Nov., Seite 1348-1354 |
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Übergeordnetes Werk: |
volume:10 ; year:2009 ; number:12 ; day:06 ; month:11 ; pages:1348-1354 |
Links: |
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DOI / URN: |
10.1038/embor.2009.236 |
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Katalog-ID: |
SPR058080708 |
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520 | |a Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. | ||
520 | |a Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. | ||
650 | 4 | |a cancer |7 (dpeaa)DE-He213 | |
650 | 4 | |a cannibalism |7 (dpeaa)DE-He213 | |
650 | 4 | |a melanoma |7 (dpeaa)DE-He213 | |
650 | 4 | |a oncogene |7 (dpeaa)DE-He213 | |
650 | 4 | |a TM9SF4 |7 (dpeaa)DE-He213 | |
700 | 1 | |a Perdicchio, Maurizio |e verfasserin |4 aut | |
700 | 1 | |a Brambilla, Daria |e verfasserin |4 aut | |
700 | 1 | |a Borghi, Martina |e verfasserin |4 aut | |
700 | 1 | |a Meschini, Stefania |e verfasserin |4 aut | |
700 | 1 | |a Barca, Stefano |e verfasserin |4 aut | |
700 | 1 | |a Marino, Maria Lucia |e verfasserin |4 aut | |
700 | 1 | |a Logozzi, Mariantonia |e verfasserin |4 aut | |
700 | 1 | |a Federici, Cristina |e verfasserin |4 aut | |
700 | 1 | |a Iessi, Elisabetta |e verfasserin |4 aut | |
700 | 1 | |a de Milito, Angelo |e verfasserin |4 aut | |
700 | 1 | |a Fais, Stefano |e verfasserin |4 aut | |
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2009 |
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10.1038/embor.2009.236 doi (DE-627)SPR058080708 (SPR)embor.2009.236-e DE-627 ger DE-627 rakwb eng Lozupone, Francesco verfasserin aut The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2009 Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. cancer (dpeaa)DE-He213 cannibalism (dpeaa)DE-He213 melanoma (dpeaa)DE-He213 oncogene (dpeaa)DE-He213 TM9SF4 (dpeaa)DE-He213 Perdicchio, Maurizio verfasserin aut Brambilla, Daria verfasserin aut Borghi, Martina verfasserin aut Meschini, Stefania verfasserin aut Barca, Stefano verfasserin aut Marino, Maria Lucia verfasserin aut Logozzi, Mariantonia verfasserin aut Federici, Cristina verfasserin aut Iessi, Elisabetta verfasserin aut de Milito, Angelo verfasserin aut Fais, Stefano verfasserin aut Enthalten in EMBO Reports Nature Publishing Group UK, 2023 10(2009), 12 vom: 06. Nov., Seite 1348-1354 (DE-627)320645622 (DE-600)2025376-X 1469-3178 nnns volume:10 year:2009 number:12 day:06 month:11 pages:1348-1354 https://dx.doi.org/10.1038/embor.2009.236 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 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_72 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_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 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_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 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_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 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_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 10 2009 12 06 11 1348-1354 |
spelling |
10.1038/embor.2009.236 doi (DE-627)SPR058080708 (SPR)embor.2009.236-e DE-627 ger DE-627 rakwb eng Lozupone, Francesco verfasserin aut The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2009 Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. cancer (dpeaa)DE-He213 cannibalism (dpeaa)DE-He213 melanoma (dpeaa)DE-He213 oncogene (dpeaa)DE-He213 TM9SF4 (dpeaa)DE-He213 Perdicchio, Maurizio verfasserin aut Brambilla, Daria verfasserin aut Borghi, Martina verfasserin aut Meschini, Stefania verfasserin aut Barca, Stefano verfasserin aut Marino, Maria Lucia verfasserin aut Logozzi, Mariantonia verfasserin aut Federici, Cristina verfasserin aut Iessi, Elisabetta verfasserin aut de Milito, Angelo verfasserin aut Fais, Stefano verfasserin aut Enthalten in EMBO Reports Nature Publishing Group UK, 2023 10(2009), 12 vom: 06. Nov., Seite 1348-1354 (DE-627)320645622 (DE-600)2025376-X 1469-3178 nnns volume:10 year:2009 number:12 day:06 month:11 pages:1348-1354 https://dx.doi.org/10.1038/embor.2009.236 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 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_72 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_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 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_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 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_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 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_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 10 2009 12 06 11 1348-1354 |
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10.1038/embor.2009.236 doi (DE-627)SPR058080708 (SPR)embor.2009.236-e DE-627 ger DE-627 rakwb eng Lozupone, Francesco verfasserin aut The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2009 Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. cancer (dpeaa)DE-He213 cannibalism (dpeaa)DE-He213 melanoma (dpeaa)DE-He213 oncogene (dpeaa)DE-He213 TM9SF4 (dpeaa)DE-He213 Perdicchio, Maurizio verfasserin aut Brambilla, Daria verfasserin aut Borghi, Martina verfasserin aut Meschini, Stefania verfasserin aut Barca, Stefano verfasserin aut Marino, Maria Lucia verfasserin aut Logozzi, Mariantonia verfasserin aut Federici, Cristina verfasserin aut Iessi, Elisabetta verfasserin aut de Milito, Angelo verfasserin aut Fais, Stefano verfasserin aut Enthalten in EMBO Reports Nature Publishing Group UK, 2023 10(2009), 12 vom: 06. Nov., Seite 1348-1354 (DE-627)320645622 (DE-600)2025376-X 1469-3178 nnns volume:10 year:2009 number:12 day:06 month:11 pages:1348-1354 https://dx.doi.org/10.1038/embor.2009.236 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 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_72 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_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 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_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 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_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 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_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 10 2009 12 06 11 1348-1354 |
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10.1038/embor.2009.236 doi (DE-627)SPR058080708 (SPR)embor.2009.236-e DE-627 ger DE-627 rakwb eng Lozupone, Francesco verfasserin aut The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2009 Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. cancer (dpeaa)DE-He213 cannibalism (dpeaa)DE-He213 melanoma (dpeaa)DE-He213 oncogene (dpeaa)DE-He213 TM9SF4 (dpeaa)DE-He213 Perdicchio, Maurizio verfasserin aut Brambilla, Daria verfasserin aut Borghi, Martina verfasserin aut Meschini, Stefania verfasserin aut Barca, Stefano verfasserin aut Marino, Maria Lucia verfasserin aut Logozzi, Mariantonia verfasserin aut Federici, Cristina verfasserin aut Iessi, Elisabetta verfasserin aut de Milito, Angelo verfasserin aut Fais, Stefano verfasserin aut Enthalten in EMBO Reports Nature Publishing Group UK, 2023 10(2009), 12 vom: 06. Nov., Seite 1348-1354 (DE-627)320645622 (DE-600)2025376-X 1469-3178 nnns volume:10 year:2009 number:12 day:06 month:11 pages:1348-1354 https://dx.doi.org/10.1038/embor.2009.236 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 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_72 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_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 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_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 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_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 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_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 10 2009 12 06 11 1348-1354 |
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10.1038/embor.2009.236 doi (DE-627)SPR058080708 (SPR)embor.2009.236-e DE-627 ger DE-627 rakwb eng Lozupone, Francesco verfasserin aut The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2009 Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. cancer (dpeaa)DE-He213 cannibalism (dpeaa)DE-He213 melanoma (dpeaa)DE-He213 oncogene (dpeaa)DE-He213 TM9SF4 (dpeaa)DE-He213 Perdicchio, Maurizio verfasserin aut Brambilla, Daria verfasserin aut Borghi, Martina verfasserin aut Meschini, Stefania verfasserin aut Barca, Stefano verfasserin aut Marino, Maria Lucia verfasserin aut Logozzi, Mariantonia verfasserin aut Federici, Cristina verfasserin aut Iessi, Elisabetta verfasserin aut de Milito, Angelo verfasserin aut Fais, Stefano verfasserin aut Enthalten in EMBO Reports Nature Publishing Group UK, 2023 10(2009), 12 vom: 06. Nov., Seite 1348-1354 (DE-627)320645622 (DE-600)2025376-X 1469-3178 nnns volume:10 year:2009 number:12 day:06 month:11 pages:1348-1354 https://dx.doi.org/10.1038/embor.2009.236 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 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_72 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_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 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_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 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_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 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_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 10 2009 12 06 11 1348-1354 |
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Enthalten in EMBO Reports 10(2009), 12 vom: 06. Nov., Seite 1348-1354 volume:10 year:2009 number:12 day:06 month:11 pages:1348-1354 |
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Lozupone, Francesco @@aut@@ Perdicchio, Maurizio @@aut@@ Brambilla, Daria @@aut@@ Borghi, Martina @@aut@@ Meschini, Stefania @@aut@@ Barca, Stefano @@aut@@ Marino, Maria Lucia @@aut@@ Logozzi, Mariantonia @@aut@@ Federici, Cristina @@aut@@ Iessi, Elisabetta @@aut@@ de Milito, Angelo @@aut@@ Fais, Stefano @@aut@@ |
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This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. 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|
author |
Lozupone, Francesco |
spellingShingle |
Lozupone, Francesco misc cancer misc cannibalism misc melanoma misc oncogene misc TM9SF4 The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells |
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1469-3178 |
topic_title |
The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells cancer (dpeaa)DE-He213 cannibalism (dpeaa)DE-He213 melanoma (dpeaa)DE-He213 oncogene (dpeaa)DE-He213 TM9SF4 (dpeaa)DE-He213 |
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misc cancer misc cannibalism misc melanoma misc oncogene misc TM9SF4 |
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misc cancer misc cannibalism misc melanoma misc oncogene misc TM9SF4 |
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misc cancer misc cannibalism misc melanoma misc oncogene misc TM9SF4 |
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title |
The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells |
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(DE-627)SPR058080708 (SPR)embor.2009.236-e |
title_full |
The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells |
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Lozupone, Francesco |
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EMBO Reports |
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eng |
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2009 |
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Lozupone, Francesco Perdicchio, Maurizio Brambilla, Daria Borghi, Martina Meschini, Stefania Barca, Stefano Marino, Maria Lucia Logozzi, Mariantonia Federici, Cristina Iessi, Elisabetta de Milito, Angelo Fais, Stefano |
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10 |
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Elektronische Aufsätze |
author-letter |
Lozupone, Francesco |
doi_str_mv |
10.1038/embor.2009.236 |
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verfasserin |
title_sort |
the human homologue of dictyostelium discoideum phg1a is expressed by human metastatic melanoma cells |
title_auth |
The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells |
abstract |
Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. © European Molecular Biology Organization 2009 |
abstractGer |
Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. © European Molecular Biology Organization 2009 |
abstract_unstemmed |
Abstract Tumour cannibalism is a characteristic of malignancy and metastatic behaviour. This atypical phagocytic activity is a crucial survival option for tumours in conditions of low nutrient supply, and has some similarities to the phagocytic activity of unicellular microorganisms. In fact, Dictyostelium discoideum has been used widely as a model to study phagocytosis. Recently, phg1A has been described as a protein that is primarily involved in the phagocytic process of this microorganism. The closest human homologue to phg1A is transmembrane 9 superfamily protein member 4 (TM9SF4). Here, we report that TM9SF4 is highly expressed in human malignant melanoma cells deriving from metastatic lesions, whereas it is undetectable in healthy human tissues and cells. TM9SF4 is predominantly expressed in acidic vesicles of melanoma cells, in which it co‐localizes with the early endosome antigens Rab5 and early endosome antigen 1. TM9SF4 silencing induced marked inhibition of cannibal activity, which is consistent with a derangement of intracellular pH gradients, with alkalinization of acidic vesicles and acidification of the cell cytosol. We propose TM9SF4 as a new marker of malignancy, representing a potential new target for anti‐tumour strategies with a specific role in tumour cannibalism and in the establishment of a metastatic phenotype. Abstract Work from the Lozupone lab shows that TM9SF4, the human homologue of phg1A, which is involved in phagocytosis in Dictyostelium discoideum, is a new tumor marker expressed by metastatic melanoma cells. The study provides evidence that TM9SF4 is involved in phagocytic activity and in derangement of intracellular pH gradients; phenomena that are typically related to the malignant phenotype of several tumors. © European Molecular Biology Organization 2009 |
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container_issue |
12 |
title_short |
The human homologue of Dictyostelium discoideum phg1A is expressed by human metastatic melanoma cells |
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https://dx.doi.org/10.1038/embor.2009.236 |
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Perdicchio, Maurizio Brambilla, Daria Borghi, Martina Meschini, Stefania Barca, Stefano Marino, Maria Lucia Logozzi, Mariantonia Federici, Cristina Iessi, Elisabetta de Milito, Angelo Fais, Stefano |
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score |
7.4007816 |