Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients
Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study en...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Zhiguo Peng [verfasserIn] Xinyue Dong [verfasserIn] Miao He [verfasserIn] Yajing Zhao [verfasserIn] Yujia Liu [verfasserIn] Mo Li [verfasserIn] Guosheng Li [verfasserIn] Xiuwen Wang [verfasserIn] Li Li [verfasserIn] Yu Hu [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
In: Thoracic Cancer - Wiley, 2015, 14(2023), 33, Seite 3282-3294 |
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| Übergeordnetes Werk: |
volume:14 ; year:2023 ; number:33 ; pages:3282-3294 |
| Links: |
Link aufrufen |
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| DOI / URN: |
10.1111/1759-7714.15119 |
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| Katalog-ID: |
DOAJ101725728 |
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| 520 | |a Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. | ||
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| 653 | 0 | |a Neoplasms. Tumors. Oncology. Including cancer and carcinogens | |
| 700 | 0 | |a Xinyue Dong |e verfasserin |4 aut | |
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| 700 | 0 | |a Yajing Zhao |e verfasserin |4 aut | |
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| 700 | 0 | |a Mo Li |e verfasserin |4 aut | |
| 700 | 0 | |a Guosheng Li |e verfasserin |4 aut | |
| 700 | 0 | |a Xiuwen Wang |e verfasserin |4 aut | |
| 700 | 0 | |a Li Li |e verfasserin |4 aut | |
| 700 | 0 | |a Yu Hu |e verfasserin |4 aut | |
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10.1111/1759-7714.15119 doi (DE-627)DOAJ101725728 (DE-599)DOAJ4758bdeaa14c4779936ea594a7c41e28 DE-627 ger DE-627 rakwb eng RC254-282 Zhiguo Peng verfasserin aut Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. breast cancer Th1 cells Th17 cells Th2 cells Th22 cells Neoplasms. Tumors. Oncology. Including cancer and carcinogens Xinyue Dong verfasserin aut Miao He verfasserin aut Yajing Zhao verfasserin aut Yujia Liu verfasserin aut Mo Li verfasserin aut Guosheng Li verfasserin aut Xiuwen Wang verfasserin aut Li Li verfasserin aut Yu Hu verfasserin aut In Thoracic Cancer Wiley, 2015 14(2023), 33, Seite 3282-3294 (DE-627)629836809 (DE-600)2559245-2 17597714 nnns volume:14 year:2023 number:33 pages:3282-3294 https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/article/4758bdeaa14c4779936ea594a7c41e28 kostenfrei https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/toc/1759-7706 Journal toc kostenfrei https://doaj.org/toc/1759-7714 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2023 33 3282-3294 |
| spelling |
10.1111/1759-7714.15119 doi (DE-627)DOAJ101725728 (DE-599)DOAJ4758bdeaa14c4779936ea594a7c41e28 DE-627 ger DE-627 rakwb eng RC254-282 Zhiguo Peng verfasserin aut Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. breast cancer Th1 cells Th17 cells Th2 cells Th22 cells Neoplasms. Tumors. Oncology. Including cancer and carcinogens Xinyue Dong verfasserin aut Miao He verfasserin aut Yajing Zhao verfasserin aut Yujia Liu verfasserin aut Mo Li verfasserin aut Guosheng Li verfasserin aut Xiuwen Wang verfasserin aut Li Li verfasserin aut Yu Hu verfasserin aut In Thoracic Cancer Wiley, 2015 14(2023), 33, Seite 3282-3294 (DE-627)629836809 (DE-600)2559245-2 17597714 nnns volume:14 year:2023 number:33 pages:3282-3294 https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/article/4758bdeaa14c4779936ea594a7c41e28 kostenfrei https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/toc/1759-7706 Journal toc kostenfrei https://doaj.org/toc/1759-7714 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2023 33 3282-3294 |
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10.1111/1759-7714.15119 doi (DE-627)DOAJ101725728 (DE-599)DOAJ4758bdeaa14c4779936ea594a7c41e28 DE-627 ger DE-627 rakwb eng RC254-282 Zhiguo Peng verfasserin aut Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. breast cancer Th1 cells Th17 cells Th2 cells Th22 cells Neoplasms. Tumors. Oncology. Including cancer and carcinogens Xinyue Dong verfasserin aut Miao He verfasserin aut Yajing Zhao verfasserin aut Yujia Liu verfasserin aut Mo Li verfasserin aut Guosheng Li verfasserin aut Xiuwen Wang verfasserin aut Li Li verfasserin aut Yu Hu verfasserin aut In Thoracic Cancer Wiley, 2015 14(2023), 33, Seite 3282-3294 (DE-627)629836809 (DE-600)2559245-2 17597714 nnns volume:14 year:2023 number:33 pages:3282-3294 https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/article/4758bdeaa14c4779936ea594a7c41e28 kostenfrei https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/toc/1759-7706 Journal toc kostenfrei https://doaj.org/toc/1759-7714 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2023 33 3282-3294 |
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10.1111/1759-7714.15119 doi (DE-627)DOAJ101725728 (DE-599)DOAJ4758bdeaa14c4779936ea594a7c41e28 DE-627 ger DE-627 rakwb eng RC254-282 Zhiguo Peng verfasserin aut Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. breast cancer Th1 cells Th17 cells Th2 cells Th22 cells Neoplasms. Tumors. Oncology. Including cancer and carcinogens Xinyue Dong verfasserin aut Miao He verfasserin aut Yajing Zhao verfasserin aut Yujia Liu verfasserin aut Mo Li verfasserin aut Guosheng Li verfasserin aut Xiuwen Wang verfasserin aut Li Li verfasserin aut Yu Hu verfasserin aut In Thoracic Cancer Wiley, 2015 14(2023), 33, Seite 3282-3294 (DE-627)629836809 (DE-600)2559245-2 17597714 nnns volume:14 year:2023 number:33 pages:3282-3294 https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/article/4758bdeaa14c4779936ea594a7c41e28 kostenfrei https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/toc/1759-7706 Journal toc kostenfrei https://doaj.org/toc/1759-7714 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2023 33 3282-3294 |
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10.1111/1759-7714.15119 doi (DE-627)DOAJ101725728 (DE-599)DOAJ4758bdeaa14c4779936ea594a7c41e28 DE-627 ger DE-627 rakwb eng RC254-282 Zhiguo Peng verfasserin aut Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. breast cancer Th1 cells Th17 cells Th2 cells Th22 cells Neoplasms. Tumors. Oncology. Including cancer and carcinogens Xinyue Dong verfasserin aut Miao He verfasserin aut Yajing Zhao verfasserin aut Yujia Liu verfasserin aut Mo Li verfasserin aut Guosheng Li verfasserin aut Xiuwen Wang verfasserin aut Li Li verfasserin aut Yu Hu verfasserin aut In Thoracic Cancer Wiley, 2015 14(2023), 33, Seite 3282-3294 (DE-627)629836809 (DE-600)2559245-2 17597714 nnns volume:14 year:2023 number:33 pages:3282-3294 https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/article/4758bdeaa14c4779936ea594a7c41e28 kostenfrei https://doi.org/10.1111/1759-7714.15119 kostenfrei https://doaj.org/toc/1759-7706 Journal toc kostenfrei https://doaj.org/toc/1759-7714 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2023 33 3282-3294 |
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Zhiguo Peng @@aut@@ Xinyue Dong @@aut@@ Miao He @@aut@@ Yajing Zhao @@aut@@ Yujia Liu @@aut@@ Mo Li @@aut@@ Guosheng Li @@aut@@ Xiuwen Wang @@aut@@ Li Li @@aut@@ Yu Hu @@aut@@ |
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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">DOAJ101725728</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20240414224141.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">240414s2023 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1111/1759-7714.15119</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ101725728</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ4758bdeaa14c4779936ea594a7c41e28</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="050" ind1=" " ind2="0"><subfield code="a">RC254-282</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Zhiguo Peng</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients</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="520" ind1=" " ind2=" "><subfield code="a">Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. 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R - Medicine |
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Zhiguo Peng |
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Zhiguo Peng misc RC254-282 misc breast cancer misc Th1 cells misc Th17 cells misc Th2 cells misc Th22 cells misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients |
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RC254-282 Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients breast cancer Th1 cells Th17 cells Th2 cells Th22 cells |
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misc RC254-282 misc breast cancer misc Th1 cells misc Th17 cells misc Th2 cells misc Th22 cells misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens |
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misc RC254-282 misc breast cancer misc Th1 cells misc Th17 cells misc Th2 cells misc Th22 cells misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens |
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Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients |
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Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients |
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elevated profiles of peripheral th22, th17, th2 cells, and decreased percentage of th1 cells in breast cancer patients |
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RC254-282 |
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Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients |
| abstract |
Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. |
| abstractGer |
Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. |
| abstract_unstemmed |
Abstract Background Th22 subset is a particular type of CD4+ T helper cells subset. Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. A negative correlation between Th1 subset and Ki‐67% as well as a positive correlation between Th2 subset and Ki‐67% was found in BC patients. The proportion of Th1 cells in BC patients was significantly lower than that of the control group. Expression of AHR and RORC transcription factors were also observed to be upregulated in the BC patients. Furthermore, Th22 cells were positively correlated with BC tumor stage and clinical outcomes. The BC patients with a higher percentage of Th22, Th17, Th1 cells or a lower percentage of Th1 cells showed a decreased trend of survival rate. Conclusion Th22, Th17, Th1, and Th2 subsets may play an essential role in BC patients. Th22, Th17, Th1, and Th2 cells may have potential significance to be used as clinical markers in BC patients with different molecular classification. Th22 cells may have potential value in BC patients’ outcomes prediction, providing clinical value. |
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Elevated profiles of peripheral Th22, Th17, Th2 cells, and decreased percentage of Th1 cells in breast cancer patients |
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https://doi.org/10.1111/1759-7714.15119 https://doaj.org/article/4758bdeaa14c4779936ea594a7c41e28 https://doaj.org/toc/1759-7706 https://doaj.org/toc/1759-7714 |
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Xinyue Dong Miao He Yajing Zhao Yujia Liu Mo Li Guosheng Li Xiuwen Wang Li Li Yu Hu |
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Xinyue Dong Miao He Yajing Zhao Yujia Liu Mo Li Guosheng Li Xiuwen Wang Li Li Yu Hu |
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2024-07-03T22:11:37.350Z |
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Our study aimed to explore the expression level of circulating Th22, Th17, Th1, and Th2 cells and the possible mechanism of these cells in breast cancer (BC) with different pathological features. Methods Our study enrolled 43 newly diagnosed BC patients and 30 healthy controls. Frequencies of peripheral Th22, Th17, Th1, and Th2 cells were tested by flow cytometry. Concentrations of IL‐22 cytokine in plasma were examined by enzyme‐linked immunosorbent assay (ELISA). Real‐time PCR was done to test aromatic hydrocarbon receptor (AHR) and RAR‐associated orphan receptor C (RORC) gene expression. Results Frequencies of Th22, Th17, Th2 subsets, and the plasma IL‐22 level was obviously higher in the BC patients. A positive correlation between Th22 frequency and IL‐22 concentration in plasma was detected in BC patients. Furthermore, the percentage of Th22, Th2 subsets in peripheral blood of HER2 positive BC was higher than that in HER2 negative BC patients. 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