author_facet Liu, Mei
Wu, Lingying
Xu, Ningzhi
An, Jusheng
Hu, Jinlong
Huang, Manni
Tu, Binbin
Hu, Chenfei
Wang, Zaozao
Zhu, Hongxia
Liu, Mei
Wu, Lingying
Xu, Ningzhi
An, Jusheng
Hu, Jinlong
Huang, Manni
Tu, Binbin
Hu, Chenfei
Wang, Zaozao
Zhu, Hongxia
author Liu, Mei
Wu, Lingying
Xu, Ningzhi
An, Jusheng
Hu, Jinlong
Huang, Manni
Tu, Binbin
Hu, Chenfei
Wang, Zaozao
Zhu, Hongxia
spellingShingle Liu, Mei
Wu, Lingying
Xu, Ningzhi
An, Jusheng
Hu, Jinlong
Huang, Manni
Tu, Binbin
Hu, Chenfei
Wang, Zaozao
Zhu, Hongxia
Cancer Prevention Research
Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
Cancer Research
Oncology
author_sort liu, mei
spelling Liu, Mei Wu, Lingying Xu, Ningzhi An, Jusheng Hu, Jinlong Huang, Manni Tu, Binbin Hu, Chenfei Wang, Zaozao Zhu, Hongxia 1940-6207 1940-6215 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1940-6207.prev-12-a19 <jats:title>Abstract</jats:title> <jats:p>Cervical cancer is one of the most common cancers in women worldwide. Advanced uterine cervical squamous cell carcinomasuterine (UCSCC) patients in FIGO stage IIb or IIIb treated with platinum based concomitant chemoradiotherapy. However, clinical outcomes vary significantly and are difficult to predict. Tumor intrinsic chemoradiotherapy sensitivity is one of the crucial reasons for concomitant chemoradiotherapy failure in UCSCC. In this study, we identified the relationship between miR-19a and sensitivity to concomitant chemoradiotherapy. The UCSCC patients in FIGO stage IIb or IIIb treated with platinum based concurrent chemoradiotherapy at the Cancer Institute and Hospital, Chinese Academy of Medical Sciences. Patients with progressive disease during first line platinum based chemotherapy or those who suffered recurrent disease within 6 months of completing first line therapy were termed resistant. Patients without recurrence or with recurrences beyond 6 months were termed sensitive. We examined the expression level of miR-19a in 30 cervix biopsies samples, including 10 resistant and 20 sensitive samples. We found miR-19a was significantly up-regulated in resistant group compared with sensitive group (p &amp;lt;0.05). Our study indicated that miR-19a might be a marker to identify cervical cancer patients who are likely to fail concomitant chemoradiotherapy. To verify role of miR-19ain cervical cancer cells is worthy of further investigation.</jats:p> <jats:p>Citation Format: Mei Liu, Lingying Wu, Ningzhi Xu, Jusheng An, Jinlong Hu, Manni Huang, Binbin Tu, Chenfei Hu, Zaozao Wang, Hongxia Zhu. miR-19a modulates chemoradiotherapy resistance in human cervical cancer. [abstract]. In: Proceedings of the Eleventh Annual AACR International Conference on Frontiers in Cancer Prevention Research; 2012 Oct 16-19; Anaheim, CA. Philadelphia (PA): AACR; Cancer Prev Res 2012;5(11 Suppl):Abstract nr A19.</jats:p> Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer Cancer Prevention Research
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series Cancer Prevention Research
source_id 49
title Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_unstemmed Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_full Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_fullStr Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_full_unstemmed Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_short Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_sort abstract a19: mir-19a modulates chemoradiotherapy resistance in human cervical cancer
topic Cancer Research
Oncology
url http://dx.doi.org/10.1158/1940-6207.prev-12-a19
publishDate 2012
physical A19-A19
description <jats:title>Abstract</jats:title> <jats:p>Cervical cancer is one of the most common cancers in women worldwide. Advanced uterine cervical squamous cell carcinomasuterine (UCSCC) patients in FIGO stage IIb or IIIb treated with platinum based concomitant chemoradiotherapy. However, clinical outcomes vary significantly and are difficult to predict. Tumor intrinsic chemoradiotherapy sensitivity is one of the crucial reasons for concomitant chemoradiotherapy failure in UCSCC. In this study, we identified the relationship between miR-19a and sensitivity to concomitant chemoradiotherapy. The UCSCC patients in FIGO stage IIb or IIIb treated with platinum based concurrent chemoradiotherapy at the Cancer Institute and Hospital, Chinese Academy of Medical Sciences. Patients with progressive disease during first line platinum based chemotherapy or those who suffered recurrent disease within 6 months of completing first line therapy were termed resistant. Patients without recurrence or with recurrences beyond 6 months were termed sensitive. We examined the expression level of miR-19a in 30 cervix biopsies samples, including 10 resistant and 20 sensitive samples. We found miR-19a was significantly up-regulated in resistant group compared with sensitive group (p &amp;lt;0.05). Our study indicated that miR-19a might be a marker to identify cervical cancer patients who are likely to fail concomitant chemoradiotherapy. To verify role of miR-19ain cervical cancer cells is worthy of further investigation.</jats:p> <jats:p>Citation Format: Mei Liu, Lingying Wu, Ningzhi Xu, Jusheng An, Jinlong Hu, Manni Huang, Binbin Tu, Chenfei Hu, Zaozao Wang, Hongxia Zhu. miR-19a modulates chemoradiotherapy resistance in human cervical cancer. [abstract]. In: Proceedings of the Eleventh Annual AACR International Conference on Frontiers in Cancer Prevention Research; 2012 Oct 16-19; Anaheim, CA. Philadelphia (PA): AACR; Cancer Prev Res 2012;5(11 Suppl):Abstract nr A19.</jats:p>
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author Liu, Mei, Wu, Lingying, Xu, Ningzhi, An, Jusheng, Hu, Jinlong, Huang, Manni, Tu, Binbin, Hu, Chenfei, Wang, Zaozao, Zhu, Hongxia
author_facet Liu, Mei, Wu, Lingying, Xu, Ningzhi, An, Jusheng, Hu, Jinlong, Huang, Manni, Tu, Binbin, Hu, Chenfei, Wang, Zaozao, Zhu, Hongxia, Liu, Mei, Wu, Lingying, Xu, Ningzhi, An, Jusheng, Hu, Jinlong, Huang, Manni, Tu, Binbin, Hu, Chenfei, Wang, Zaozao, Zhu, Hongxia
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description <jats:title>Abstract</jats:title> <jats:p>Cervical cancer is one of the most common cancers in women worldwide. Advanced uterine cervical squamous cell carcinomasuterine (UCSCC) patients in FIGO stage IIb or IIIb treated with platinum based concomitant chemoradiotherapy. However, clinical outcomes vary significantly and are difficult to predict. Tumor intrinsic chemoradiotherapy sensitivity is one of the crucial reasons for concomitant chemoradiotherapy failure in UCSCC. In this study, we identified the relationship between miR-19a and sensitivity to concomitant chemoradiotherapy. The UCSCC patients in FIGO stage IIb or IIIb treated with platinum based concurrent chemoradiotherapy at the Cancer Institute and Hospital, Chinese Academy of Medical Sciences. Patients with progressive disease during first line platinum based chemotherapy or those who suffered recurrent disease within 6 months of completing first line therapy were termed resistant. Patients without recurrence or with recurrences beyond 6 months were termed sensitive. We examined the expression level of miR-19a in 30 cervix biopsies samples, including 10 resistant and 20 sensitive samples. We found miR-19a was significantly up-regulated in resistant group compared with sensitive group (p &amp;lt;0.05). Our study indicated that miR-19a might be a marker to identify cervical cancer patients who are likely to fail concomitant chemoradiotherapy. To verify role of miR-19ain cervical cancer cells is worthy of further investigation.</jats:p> <jats:p>Citation Format: Mei Liu, Lingying Wu, Ningzhi Xu, Jusheng An, Jinlong Hu, Manni Huang, Binbin Tu, Chenfei Hu, Zaozao Wang, Hongxia Zhu. miR-19a modulates chemoradiotherapy resistance in human cervical cancer. [abstract]. In: Proceedings of the Eleventh Annual AACR International Conference on Frontiers in Cancer Prevention Research; 2012 Oct 16-19; Anaheim, CA. Philadelphia (PA): AACR; Cancer Prev Res 2012;5(11 Suppl):Abstract nr A19.</jats:p>
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spelling Liu, Mei Wu, Lingying Xu, Ningzhi An, Jusheng Hu, Jinlong Huang, Manni Tu, Binbin Hu, Chenfei Wang, Zaozao Zhu, Hongxia 1940-6207 1940-6215 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1940-6207.prev-12-a19 <jats:title>Abstract</jats:title> <jats:p>Cervical cancer is one of the most common cancers in women worldwide. Advanced uterine cervical squamous cell carcinomasuterine (UCSCC) patients in FIGO stage IIb or IIIb treated with platinum based concomitant chemoradiotherapy. However, clinical outcomes vary significantly and are difficult to predict. Tumor intrinsic chemoradiotherapy sensitivity is one of the crucial reasons for concomitant chemoradiotherapy failure in UCSCC. In this study, we identified the relationship between miR-19a and sensitivity to concomitant chemoradiotherapy. The UCSCC patients in FIGO stage IIb or IIIb treated with platinum based concurrent chemoradiotherapy at the Cancer Institute and Hospital, Chinese Academy of Medical Sciences. Patients with progressive disease during first line platinum based chemotherapy or those who suffered recurrent disease within 6 months of completing first line therapy were termed resistant. Patients without recurrence or with recurrences beyond 6 months were termed sensitive. We examined the expression level of miR-19a in 30 cervix biopsies samples, including 10 resistant and 20 sensitive samples. We found miR-19a was significantly up-regulated in resistant group compared with sensitive group (p &amp;lt;0.05). Our study indicated that miR-19a might be a marker to identify cervical cancer patients who are likely to fail concomitant chemoradiotherapy. To verify role of miR-19ain cervical cancer cells is worthy of further investigation.</jats:p> <jats:p>Citation Format: Mei Liu, Lingying Wu, Ningzhi Xu, Jusheng An, Jinlong Hu, Manni Huang, Binbin Tu, Chenfei Hu, Zaozao Wang, Hongxia Zhu. miR-19a modulates chemoradiotherapy resistance in human cervical cancer. [abstract]. In: Proceedings of the Eleventh Annual AACR International Conference on Frontiers in Cancer Prevention Research; 2012 Oct 16-19; Anaheim, CA. Philadelphia (PA): AACR; Cancer Prev Res 2012;5(11 Suppl):Abstract nr A19.</jats:p> Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer Cancer Prevention Research
spellingShingle Liu, Mei, Wu, Lingying, Xu, Ningzhi, An, Jusheng, Hu, Jinlong, Huang, Manni, Tu, Binbin, Hu, Chenfei, Wang, Zaozao, Zhu, Hongxia, Cancer Prevention Research, Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer, Cancer Research, Oncology
title Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_full Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_fullStr Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_full_unstemmed Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_short Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
title_sort abstract a19: mir-19a modulates chemoradiotherapy resistance in human cervical cancer
title_unstemmed Abstract A19: miR-19a modulates chemoradiotherapy resistance in human cervical cancer
topic Cancer Research, Oncology
url http://dx.doi.org/10.1158/1940-6207.prev-12-a19