Down-regulation of SNX1 predicts poor prognosis and contributes to drug resistance in colorectal cancer
As a potential tumor suppressor, the detailed clinical application value of sorting nexin 1 (SNX1) has not been elucidated in colorectal cancer (CRC). The aim of the present study was to evaluate the expression of SNX1 in CRC tissues and to determine its correlation with clinicopathologic characteri...
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| Published in: | Tumor biology Vol. 37; no. 5; pp. 6619 - 6625 |
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| Main Authors: | , , , , , , , , , , |
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01.05.2016
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| ISSN: | 1010-4283, 1423-0380 |
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| Abstract | As a potential tumor suppressor, the detailed clinical application value of sorting nexin 1 (SNX1) has not been elucidated in colorectal cancer (CRC). The aim of the present study was to evaluate the expression of SNX1 in CRC tissues and to determine its correlation with clinicopathologic characteristics and its impact on patient’s prognosis. We detected the expression of SNX1 mRNA in 72 CRC patients and SNX1 protein in 237 CRC patients by real-time polymerase chain reaction (RT-PCR) and immunohistochemical staining, respectively. Relationship between the expression of SNX1 and various clinicopathological features in these patients was evaluated. Both the mRNA and protein expression of SNX1 were remarkably decreased in CRC tissues compared with paired non-cancerous tissues, and the down-regulation of SNX1 protein was strongly associated with poor differentiation and poor overall survival (OS) rate of CRC patients. Ectopic SNX1 expression repressed CRC cell growth and promoted tumor sensitivity to most commonly used chemotherapeutic drugs (oxaliplatin and 5-Fluorouracil). In conclusion, overexpression of SNX1 may serve as a new therapeutic strategy for CRC. |
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| AbstractList | As a potential tumor suppressor, the detailed clinical application value of sorting nexin 1 (SNX1) has not been elucidated in colorectal cancer (CRC). The aim of the present study was to evaluate the expression of SNX1 in CRC tissues and to determine its correlation with clinicopathologic characteristics and its impact on patient's prognosis. We detected the expression of SNX1 mRNA in 72 CRC patients and SNX1 protein in 237 CRC patients by real-time polymerase chain reaction (RT-PCR) and immunohistochemical staining, respectively. Relationship between the expression of SNX1 and various clinicopathological features in these patients was evaluated. Both the mRNA and protein expression of SNX1 were remarkably decreased in CRC tissues compared with paired non-cancerous tissues, and the down-regulation of SNX1 protein was strongly associated with poor differentiation and poor overall survival (OS) rate of CRC patients. Ectopic SNX1 expression repressed CRC cell growth and promoted tumor sensitivity to most commonly used chemotherapeutic drugs (oxaliplatin and 5-Fluorouracil). In conclusion, overexpression of SNX1 may serve as a new therapeutic strategy for CRC. |
| Author | Feng, Yuyang Bian, Zehua Zhou, Leyuan Gu, Bing Liu, Zhihui Hu, Yaling Xue, Yao Wang, Qifeng Zhang, Jiwei Yin, Yuan Huang, Zhaohui |
| Author_xml | – sequence: 1 givenname: Zehua surname: Bian fullname: Bian, Zehua organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 2 givenname: Yuyang surname: Feng fullname: Feng, Yuyang organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 3 givenname: Yao surname: Xue fullname: Xue, Yao organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 4 givenname: Yaling surname: Hu fullname: Hu, Yaling organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 5 givenname: Qifeng surname: Wang fullname: Wang, Qifeng organization: Department of Pathology, Fudan University Shanghai Cancer Center – sequence: 6 givenname: Leyuan surname: Zhou fullname: Zhou, Leyuan organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 7 givenname: Zhihui surname: Liu fullname: Liu, Zhihui organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 8 givenname: Jiwei surname: Zhang fullname: Zhang, Jiwei organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 9 givenname: Yuan surname: Yin fullname: Yin, Yuan organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University – sequence: 10 givenname: Bing surname: Gu fullname: Gu, Bing organization: Department of Laboratory Medicine, Affiliated Hospital of Xuzhou Medical College, Medical Technology Institute of Xuzhou Medical College – sequence: 11 givenname: Zhaohui surname: Huang fullname: Huang, Zhaohui email: hzhwxsy@126.com organization: Wuxi Oncology Institute, The Affiliated Hospital of Jiangnan University |
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| Keywords | Sorting nexin 1 (SNX1) Prognosis Drug resistance Colorectal cancer (CRC) |
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| SubjectTerms | Adult Aged Antineoplastic Agents - pharmacology Biomarkers, Tumor Biomedical and Life Sciences Biomedicine Cancer Research Cell Line, Tumor Cell Proliferation Colorectal cancer Colorectal Neoplasms - genetics Colorectal Neoplasms - mortality Colorectal Neoplasms - pathology Down-Regulation Drug resistance Drug Resistance, Neoplasm - genetics Female Fluorouracil - pharmacology Gene Expression Regulation, Neoplastic Humans Kaplan-Meier Estimate Lymphatic Metastasis Male Medical prognosis Middle Aged Neoplasm Grading Neoplasm Staging Original Article Prognosis Sorting Nexins - genetics Studies Tumor Burden Tumors |
| Title | Down-regulation of SNX1 predicts poor prognosis and contributes to drug resistance in colorectal cancer |
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