KIAA1549 promotes the development and chemoresistance of colorectal cancer by upregulating ERCC2

被引:1
作者
Ye, Feng [1 ]
Xie, Yuwen [1 ]
Lin, Mingdao [2 ,3 ]
Liu, Yang [1 ]
Fang, Yuan [1 ]
Chen, Keli [4 ]
Zhang, Yaowei [1 ]
Ding, Yi [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Radiat Oncol, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Sch Clin Med 1, Dept Gen Surg, Guangzhou 510515, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Sch Clin Med 1, Guangdong Prov Key Lab Precis Med Gastrointestinal, Guangzhou 510515, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Huiqiao Med Ctr, Guangzhou 510515, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorectal cancer; KIAA1549; Development; Chemotherapy; Chemoresistance; NUCLEOTIDE EXCISION-REPAIR; MESSENGER-RNA LEVELS; FUSION GENE; PHASE-II; CISPLATIN; DNA; PATHWAY; POLYMORPHISMS; FLUOROURACIL; CHEMOTHERAPY;
D O I
10.1007/s11010-023-04751-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Colorectal cancer (CRC) is the third most commonly diagnosed cancer worldwide. Chemotherapy is the mainstay of treatment for patients with CRC in II-IV stages. Resistance to chemotherapy occurs commonly, which results in treatment failure. Therefore, the identification of novel functional biomarkers is essential for recognizing high-risk patients, predicting recurrence, and developing new therapeutic strategies. Herein, we assessed the roles of KIAA1549 in promoting tumor development and chemoresistance in colorectal cancer. As a result, we found that KIAA1549 expression is up-regulation in CRC. Public databases revealed a progressive up-regulation of KIAA1549 expression from adenomas to carcinomas. Functional characterization uncovered that KIAA1549 promotes tumor malignant phenotypes and boosts the chemoresistance of CRC cells in an ERCC2-dependent manner. Inhibition of KIAA1549 and ERCC2 effectively enhanced the sensitivity to chemotherapeutic drugs oxaliplatin and 5-fluorouracil. Our findings suggest that endogenous KIAA1549 might function as a tumor development-promoting role and trigger chemoresistance in colorectal cancer partly by upregulating DNA repair protein ERCC2. Hence, KIAA1549 could be an effective therapeutic target for CRC and inhibition of KIAA1549 combined with chemotherapy might be a potential therapeutic strategy in the future.
引用
收藏
页码:629 / 642
页数:14
相关论文
共 35 条
[1]   KIAA1549:BRAF Fusion Gene in Pediatric Brain Tumors of Various Histogenesis [J].
Antonelli, Manila ;
Badiali, Manuela ;
Moi, Loredana ;
Buttarelli, Francesca R. ;
Baldi, Caterina ;
Massimino, Maura ;
Sanson, Marc ;
Giangaspero, Felice .
PEDIATRIC BLOOD & CANCER, 2015, 62 (04) :724-727
[2]   Genetic variation in the nucleotide excision repair pathway and colorectal cancer risk [J].
Berndt, Sonja I. ;
Platz, Elizabeth A. ;
Fallin, M. Daniele ;
Thuita, Lucy W. ;
Hoffman, Sandra C. ;
Helzlsouer, Kathy J. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (11) :2263-2269
[3]   Association Between Time to Initiation of Adjuvant Chemotherapy and Survival in Colorectal Cancer A Systematic Review and Meta-analysis [J].
Biagi, James J. ;
Raphael, Michael J. ;
Mackillop, William J. ;
Kong, Weidong ;
King, Will D. ;
Booth, Christopher M. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2011, 305 (22) :2335-2342
[4]   Association Between ERCC1 rs3212986 and ERCC2/XPD rs1799793 and OS in Patients With Advanced Esophageal Cancer [J].
Boldrin, Elisa ;
Malacrida, Sandro ;
Rumiato, Enrica ;
Battaglia, Giorgio ;
Ruol, Alberto ;
Amadori, Alberto ;
Saggioro, Daniela .
FRONTIERS IN ONCOLOGY, 2019, 9
[5]   KIAA1549-BRAF Expression Establishes a Permissive Tumor Microenvironment Through NFκB-Mediated CCL2 Production [J].
Chen, Ran ;
Keoni, Chanel ;
Waker, Christopher A. ;
Lober, Robert M. ;
Gutmann, David H. .
NEOPLASIA, 2019, 21 (01) :52-60
[6]   MESSENGER-RNA LEVELS OF XPAC AND ERCC1 IN OVARIAN-CANCER TISSUE CORRELATE WITH RESPONSE TO PLATINUM-BASED CHEMOTHERAPY [J].
DABHOLKAR, M ;
VIONNET, J ;
BOSTICKBRUTON, F ;
YU, JJ ;
REED, E .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :703-708
[7]   Expression of genes involved in nucleotide excision repair and sensitivity to cisplatin and melphalan in human cancer cell lines [J].
Damia, G ;
Guidi, G ;
D'Incalci, M .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (11) :1783-1788
[8]   Role of Endonucleases XPF and XPG in Nucleotide Excision Repair of Platinated DNA and Cisplatin/Oxaliplatin Cytotoxicity [J].
Graf, Nora ;
Ang, Wee Han ;
Zhu, Guangyu ;
Myint, MyatNoeZin ;
Lippard, Stephen J. .
CHEMBIOCHEM, 2011, 12 (07) :1115-1123
[9]   Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019 Featured Updates to the NCCN Guidelines [J].
Gupta, Samir ;
Provenzale, Dawn ;
Llor, Xavier ;
Halverson, Amy L. ;
Grady, William ;
Chung, Daniel C. ;
Haraldsdottir, Sigurdis ;
Markowitz, Arnold J. ;
Slavin, Thomas P., Jr. ;
Hampel, Heather ;
Ness, Reid M. ;
Weiss, Jennifer M. ;
Ahnen, Dennis J. ;
Chen, Lee-may ;
Cooper, Gregory ;
Early, Dayna S. ;
Giardiello, Francis M. ;
Hall, Michael J. ;
Hamilton, Stanley R. ;
Kanth, Priyanka ;
Klapman, Jason B. ;
Lazenby, Audrey J. ;
Lynch, Patrick M. ;
Mayer, Robert J. ;
Mikkelson, June ;
Peter, Shajan ;
Regenbogen, Scott E. ;
Dwyer, Mary A. ;
Ogba, Ndiya .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2019, 17 (09) :1033-1041
[10]   XPD and XRCC1 genetic polymorphisms are prognostic factors in advanced non-small-cell lung cancer patients treated with platinum chemotherapy [J].
Gurubhagavatula, S ;
Liu, G ;
Park, S ;
Zhou, W ;
Su, L ;
Wain, JC ;
Lynch, TJ ;
Neuberg, DS ;
Christiani, DC .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (13) :2594-2601