DEPDC1B promotes colorectal cancer via facilitating cell proliferation and migration while inhibiting apoptosis

被引:8
作者
Han, Fei [1 ]
Cheng, Chao [1 ]
Xu, Qianqian [2 ]
Chen, Jisong [4 ]
Yang, Zhaohui [3 ]
Liu, Jun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Gastrointestinal Surg, 1277 Jiefang St, Wuhan 430022, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Pediat, Wuhan, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Rehabil, 1277 Jiefang St, Wuhan 430022, Hubei, Peoples R China
[4] China Three Gorges Univ, Coll Clin Med Sci 2, Yichang, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorectal cancer; DEPDC1B; apoptosis; proliferation; migration; FOLFIRI PLUS BEVACIZUMAB; DEP-DOMAIN; 1ST-LINE TREATMENT; OPEN-LABEL; PROTEINS; SURVIVAL; INVASION; BINDING; GROWTH;
D O I
10.1080/15384101.2022.2110439
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Colorectal cancer (CRC) is a common malignant tumor with strong invasiveness. Given the reported involvement of DEP domain-containing protein 1B (DEPDC1B) in the progression of some cancers, its role in CRC was explored in this study. DEPDC1B expression in CRC was assessed based on database and tissue microarray (TMA). In addition, the knockdown and overexpression of DEPDC1B in CRC cell lines were constructed using small hairpin RNA (shRNA) interference. The biological function of DEPDC1B in CRC was evaluated in vitro and in vivo through loss/gain-of-function assays. The results demonstrated that DEPDC1B was highly expressed in CRC. Furthermore, DEPDC1B had the ability to promote CRC proliferation and migration coupled by cell apoptosis. In vivo results showed that DEPDC1B knockdown significantly inhibited the growth of xenograft tumors. Additionally, the results of antibody array indicated increased apoptosis-promoting proteins and decreased apoptosis-inhibiting proteins in DEPDC1B-knockdown CRC cells. In conclusion, DEPDC1B played a key driver role in CRC progression, and inhibition of its expression may be a potential target for precision medicine in CRC.
引用
收藏
页码:131 / 143
页数:13
相关论文
共 34 条
[1]   High levels of DEPDC1B predict shorter biochemical recurrence-free survival of patients with prostate cancer [J].
Bai, Shoumin ;
Chen, Ting ;
Du, Tao ;
Chen, Xianju ;
Lai, Yiming ;
Ma, Xiaoming ;
Wu, Wanhua ;
Lin, Chunhao ;
Liu, Leyuan ;
Huang, Hai .
ONCOLOGY LETTERS, 2017, 14 (06) :6801-6808
[2]  
Ballon DR, 2006, CELL, V126, P1079, DOI 10.1016/j.cell.2006.07.030
[3]   Molecular spectrum of KRAS, BRAF, and PIK3CA gene mutation: determination of frequency, distribution pattern in Indian colorectal carcinoma [J].
Bisht, Swati ;
Ahmad, Firoz ;
Sawaimoon, Satyakam ;
Bhatia, Simi ;
Das, Bibhu Ranjan .
MEDICAL ONCOLOGY, 2014, 31 (09) :1-13
[4]  
Boudreau HE, 2007, INT J MOL MED, V19, P29
[5]   Interplay between diet, gut microbiota, epigenetic events, and colorectal cancer [J].
Bultman, Scott J. .
MOLECULAR NUTRITION & FOOD RESEARCH, 2017, 61 (01)
[6]   Regulators of G protein signaling: A bestiary of modular protein binding domains [J].
Burchett, SA .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (04) :1335-1351
[7]  
Cancer Genome Atlas Network, 2012, Nature, V487, P330, DOI [10.1038/nature11252, DOI 10.1038/NATURE11252]
[8]   DEP domains: More than just membrane anchors [J].
Chen, Songhai ;
Hamm, Heidi E. .
DEVELOPMENTAL CELL, 2006, 11 (04) :436-438
[9]   Knockdown of DEPDC1B inhibits the development of glioblastoma [J].
Chen, Xu ;
Guo, Zheng-Qian ;
Cao, Dan ;
Chen, Yong ;
Chen, Jian .
CANCER CELL INTERNATIONAL, 2020, 20 (01)
[10]   Colonoscopic surveillance: quality, guidelines and effectiveness [J].
Chittleborough, Timothy J. ;
Kong, Joseph C. ;
Guerra, Glen R. ;
Ramsay, Robert ;
Heriot, Alexander G. .
ANZ JOURNAL OF SURGERY, 2018, 88 (1-2) :32-38