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Published on: May 17, 2019
BIN1 in cancer: biomarker and therapeutic target
Si-Yu Chen1, Jin-Long Cao1, Kun-Peng Li1
1Department of Urology, The Second Hospital of Lanzhou University, Lanzhou, China.
Background:
The bridging integrator 1 (BIN1) protein was originally identified as a pro-apoptotic tumor suppressor that binds to and inhibits oncogenic MYC transcription factors. BIN1 has complex physiological functions participating in endocytosis, membrane cycling, cytoskeletal regulation, DNA repair deficiency, cell-cycle arrest, and apoptosis. The expression of BIN1 is closely related to the development of various diseases such as cancer, Alzheimer's disease, myopathy, heart failure, and inflammation.
Purpose:
Because BIN1 is commonly expressed in terminally differentiated normal tissues and is usually undetectable in refractory or metastatic cancer tissues, this differential expression has led us to focus on human cancers associated with BIN1. In this review, we discuss the potential pathological mechanisms of BIN1 during cancer development and its feasibility as a prognostic marker and therapeutic target for related diseases based on recent findings on its molecular, cellular, and physiological roles.
Conclusion:
BIN1 is a tumor suppressor that regulates cancer development through a series of signals in tumor progression and microenvironment. It also makes BIN1 a feasible early diagnostic or prognostic marker for cancer.
Insights
Bridging integrator 1 (BIN1) acts as a tumor suppressor, regulating cancer progression. Its differential expression suggests BIN1 is a potential prognostic marker for human cancers.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Bridging integrator 1 (BIN1) functions as a pro-apoptotic tumor suppressor, inhibiting MYC transcription factors.
- BIN1 plays roles in endocytosis, membrane cycling, cytoskeletal regulation, DNA repair, cell-cycle arrest, and apoptosis.
- BIN1 expression is linked to cancer, Alzheimer's disease, myopathy, heart failure, and inflammation.
Purpose of the Study:
- To review the pathological mechanisms of BIN1 in human cancer development.
- To evaluate BIN1's potential as a prognostic marker and therapeutic target in cancers.
- Focus on differential expression of BIN1 in normal versus cancerous tissues.
Main Methods:
- Literature review of recent findings on BIN1's molecular, cellular, and physiological roles.
- Analysis of BIN1's involvement in cancer progression and the tumor microenvironment.
- Examination of BIN1's expression patterns in various human cancers.
Main Results:
- BIN1 is typically expressed in normal differentiated tissues but undetectable in metastatic cancers.
- BIN1 acts as a tumor suppressor, influencing cancer development through various signaling pathways.
- BIN1's distinct expression profile supports its role in tumor progression.
Conclusions:
- BIN1 is a crucial tumor suppressor regulating cancer development and the tumor microenvironment.
- BIN1's differential expression makes it a feasible marker for early cancer diagnosis and prognosis.
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