RNA interference-mediated knockdown of tripartite motif containing 44 suppresses cervical cancer growth in vitro and in vivo

被引:0
作者
Liu, Rui [1 ]
Ma, Yanan [1 ]
Gu, Wenli [1 ]
Song, Canxu [2 ]
Zhou, Lina [1 ]
Meng, Huanran [1 ]
Zhang, Yuan [1 ]
Yang, Caihong [1 ]
机构
[1] Ningxia Med Univ, Hosp Cardiovasc & Cerebrovasc Dis, Dept Gynecol, Gen Hosp, 804 Shengli St, Yinchuan 750002, Ningxia, Peoples R China
[2] Xi An Jiao Tong Univ, Shaanxi Prov Canc Hosp, Dept Ultrasound Med, Xian 710061, Shaanxi, Peoples R China
关键词
Tripartite motif containing 44; Cervical cancer; Growth; Apoptosis; Invasion; Migration; beta-Catenin; CELL-PROLIFERATION; TRIM44; INVASION; MIGRATION;
D O I
10.1007/s13273-021-00218-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Tripartite motif containing 44 (TRIM44) is an atypical member of the TRIM protein family that has been reported to be aberrantly overexpressed in multiple human cancers, including cervical cancer. Nonetheless, the potential role of TRIM44 in cervical cancer development has not yet been determined. Objective In this study, we used an RNA interference approach to knockdown endogenous TRIM44 expression in human cervical cancer HeLa and SiHa cells, and stable cells with TRIM44 knockdown were obtained. Result TRIM44 knockdown significantly inhibited cell growth, invasion and migration, whereas induced spontaneous apoptosis in HeLa and SiHa cells. Cells with stable TRIM44 knockdown exhibited reduced levels of Cyclin D1, Bcl-2, c-Myc and beta-Catenin, but elevated levels of cleaved Caspase-3 and Bax in comparison to those transfected with a control vector. In vivo, nude mice injected with stable TRIM44 knockdown HeLa or SiHa cells showed reduced tumor growth than that in control cells. Conclusion Taken together, TRIM44 is involved in tumorigenesis of cervical cancer and may represent a novel molecular target for cervical cancer prevention and therapy.
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页数:9
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共 30 条
[1]   Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis [J].
Arbyn, Marc ;
Weiderpass, Elisabete ;
Bruni, Laia ;
de Sanjose, Silvia ;
Saraiya, Mona ;
Ferlay, Jacques ;
Bray, Freddie .
LANCET GLOBAL HEALTH, 2020, 8 (02) :E191-E203
[2]   Isolation of a mouse brain cDNA expressed in developing neuroblasts and mature neurons [J].
Boutou, E ;
Matsas, R ;
Mamalaki, A .
MOLECULAR BRAIN RESEARCH, 2001, 86 (1-2) :153-167
[3]   Klotho inhibits the capacity of cell migration and invasion in cervical cancer [J].
Chang, Boogi ;
Kim, Jinsun ;
Jeong, Dongjun ;
Jeong, Yujun ;
Jeon, Seob ;
Jung, Sam-Il ;
Yang, Young ;
Kim, Keun Il ;
Lim, Jong-Seok ;
Kim, Changjin ;
Lee, Myeong-Sok .
ONCOLOGY REPORTS, 2012, 28 (03) :1022-1028
[4]   Inhibition of SPATS2 Suppresses Proliferation and Invasion of Hepatocellular Carcinoma Cells through TRIM44-STAT3 Signaling Pathway [J].
Chen, Lirong ;
Yi, Chenhe ;
Li, Wenshuai ;
Tseng, Yujen ;
Zhang, Jun ;
Liu, Jie .
JOURNAL OF CANCER, 2021, 12 (01) :89-98
[5]   Human papillomavirus and cervical cancer [J].
Crosbie, Emma J. ;
Einstein, Mark H. ;
Franceschi, Silvia ;
Kitchener, Henry C. .
LANCET, 2013, 382 (9895) :889-899
[6]   MicroRNA-623 Inhibits Epithelial-Mesenchymal Transition to Attenuate Glioma Proliferation by Targeting TRIM44 [J].
Cui, Dawei ;
Wang, Kaijie ;
Liu, Yan ;
Gao, Junling ;
Cui, Jianzhong .
ONCOTARGETS AND THERAPY, 2020, 13 :9291-9303
[7]   TRIM44 promotes human esophageal cancer progression via the AKT/mTOR pathway [J].
Dian Xiong ;
Chun Jin ;
Ye, Xudong ;
Qiu, Baiquan ;
Xu Jianjun ;
Zhu, Shuqiang ;
Long Xiang ;
Wu, Haibo ;
Wu Yongbing .
CANCER SCIENCE, 2018, 109 (10) :3080-3092
[8]   TRIM proteins and cancer [J].
Hatakeyama, Shigetsugu .
NATURE REVIEWS CANCER, 2011, 11 (11) :792-804
[9]   Overexpression of TRIM44 contributes to malignant outcome in gastric carcinoma [J].
Kashimoto, Kingo ;
Komatsu, Shuhei ;
Ichikawa, Daisuke ;
Arita, Tomohiro ;
Konishi, Hirotaka ;
Nagata, Hiroaki ;
Takeshita, Hiroki ;
Nishimura, Yukihisa ;
Hirajima, Shoji ;
Kawaguchi, Tsutomu ;
Shiozaki, Atsushi ;
Fujiwara, Hitoshi ;
Okamoto, Kazuma ;
Tsuda, Hitoshi ;
Otsuji, Eigo .
CANCER SCIENCE, 2012, 103 (11) :2021-2026
[10]   TRIM44 Is a Poor Prognostic Factor for Breast Cancer Patients as a Modulator of NF-B Signaling [J].
Kawabata, Hidetaka ;
Azuma, Kotaro ;
Ikeda, Kazuhiro ;
Sugitani, Ikuko ;
Kinowaki, Keiichi ;
Fujii, Takeshi ;
Osaki, Akihiko ;
Saeki, Toshiaki ;
Horie-Inoue, Kuniko ;
Inoue, Satoshi .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (09)