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BTG2: a rising star of tumor suppressors (review)
Bijing Mao1, Zhimin Zhang1, Ge Wang1
1Cancer Center, Institute of Surgical Research, Daping Hospital, Third Military Medical University, Chongqing 400042, P.R. China.
Abstract:
B-cell translocation gene 2 (BTG2), the first gene identified in the BTG/TOB gene family, is involved in many biological activities in cancer cells acting as a tumor suppressor. The BTG2 expression is downregulated in many human cancers. It is an instantaneous early response gene and plays important roles in cell differentiation, proliferation, DNA damage repair, and apoptosis in cancer cells. Moreover, BTG2 is regulated by many factors involving different signal pathways. However, the regulatory mechanism of BTG2 is largely unknown. Recently, the relationship between microRNAs and BTG2 has attracted much attention. MicroRNA-21 (miR-21) has been found to regulate BTG2 gene during carcinogenesis. In this review, we summarize the latest findings in the investigations of biological functions of BTG2 and regulation of its expression, with an emphasis on miR-21 in regulation of BTG2 gene in various cancers. B-cell translocation gene 2 (BTG2), also known as PC3 or TIS21, belongs to the antiproliferative (APRO) gene family. Several studies have demonstrated that BTG2 is involved in a large number of physiological and pathological processes, such as cell differentiation, proliferation, apoptosis, and other cellular functions, acting as a tumor suppressor. In this review, we summarize the latest findings in BTG2 studies, highlighting the mechanisms for the regulatory effects of microRNAs (miRNAs) on BTG2 gene expression in the most common human cancers.
Insights
B-cell translocation gene 2 (BTG2) acts as a tumor suppressor, but its expression decreases in many cancers. MicroRNA-21 (miR-21) is a key regulator of BTG2, impacting cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- B-cell translocation gene 2 (BTG2) is a tumor suppressor involved in cell differentiation, proliferation, DNA repair, and apoptosis.
- BTG2 expression is frequently downregulated in human cancers, suggesting a role in carcinogenesis.
- The precise regulatory mechanisms controlling BTG2 expression remain largely unelucidated.
Purpose of the Study:
- To review the biological functions of BTG2 in cancer cells.
- To summarize recent findings on the regulation of BTG2 expression.
- To highlight the role of microRNA-21 (miR-21) in modulating BTG2 gene expression across various cancers.
Main Methods:
- Literature review of studies investigating BTG2 function and regulation.
- Analysis of research focusing on microRNA interactions with BTG2.
- Synthesis of data on BTG2's role in different human cancer types.
Main Results:
- BTG2 exhibits diverse biological activities, including antiproliferative effects, functioning as a tumor suppressor.
- MicroRNAs, particularly miR-21, have emerged as significant regulators of BTG2 expression.
- Dysregulation of the miR-21/BTG2 axis is implicated in the development and progression of common human cancers.
Conclusions:
- BTG2 plays a critical role in tumor suppression through its involvement in fundamental cellular processes.
- MicroRNA-mediated regulation, especially by miR-21, is a key mechanism influencing BTG2 levels in cancer.
- Understanding the miR-21-BTG2 interaction offers potential therapeutic strategies for cancer treatment.
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