A Number of the N-terminal RASSF Family: RASSF7

被引:0
|
作者
Xu, Yang [1 ,2 ]
Du, Wei [3 ]
Xiao, Yongshuang [1 ]
Gao, Keyu [1 ]
Li, Jie [1 ]
Li, Shuofeng [1 ]
机构
[1] Xuzhou Med Univ, Affiliated Hosp, Dept Urol, Xuzhou 221002, Peoples R China
[2] Huzhou Cent Hosp, Dept Urol, Huzhou 313000, Zhejiang, Peoples R China
[3] Wanbei Coal Elect Grp Gen Hosp, Dept Urol, Suzhou 234000, Peoples R China
关键词
RASSF7; tumor promoter; therapeutic target; malignancy; CpG islands; N-terminal; DOMAIN-CONTAINING PROTEINS; AURORA-B ACTIVATION; SIGNALING PATHWAY; INNER CENTROMERE; BREAST-CANCER; C-MYC; ASSOCIATION; GENES; RISK; ONCOGENES;
D O I
10.2174/1871520622666220930094149
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Ras association domain family 7 (RASSF7, also named HRC1), a potential tumor-related gene, located on human chromosome 11p15, has been identified as an important member of the N-terminal RASSF family. Whereas, the molecular biological mechanisms of RASSF7 in tumorigenesis remain to be further established. We perform a systematic review of the literature and assessment from PUBMED and MEDLINE databases in this article. RASSF7 plays a significant role in mitosis, microtubule growth, apoptosis, proliferation and differentiation. Many research literature shows that the RASSF7 could promote the occurrence and advance of human tumors by regulating Aurora B, MKK4, MKK7, JNK, YAP, MEK, and ERK, whereas, it might inhibit c-Myc and thus lead to the suppression of tumorigenesis.The pregulation of RASSF7 often occurs in various malignancies such as lung cancer, neuroblastoma, thyroid neoplasm, hepatocellular cancer, breast cancer and gastric cancer. The expression stage of RASSF7 is positively correlated with the tumor TNM stage. In this review, we primarily elaborate on the acknowledged structure and progress in the various biomechanisms and research advances of RASSF7, especially the potential relevant signaling pathways. We hope that RASSF7, a prospective therapeutic target for human malignancies, could play an available role in future anti-cancer treatment.
引用
收藏
页码:889 / 895
页数:7
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