Target Name: BCAR1
NCBI ID: G9564
Review Report on BCAR1 Target / Biomarker Content of Review Report on BCAR1 Target / Biomarker
BCAR1
Other Name(s): CAS1 | BCAR1_HUMAN | Cas scaffolding protein family member 1 | CRKAS | CAS | CASS1 | Crk-associated substrate | Breast cancer anti-estrogen resistance 1 | BCAR1 scaffold protein, Cas family member | BCAR1 scaffold protein, Cas family member, transcript variant 1 | Breast cancer anti-estrogen resistance protein 1 (isoform 6) | BCAR1 scaffold protein, Cas family member, transcript variant 6 | BCAR1 variant 6 | Breast cancer anti-estrogen resistance protein 1 | p130cas | BCAR1 variant 1 | Breast cancer anti-estrogen resistance protein 1 (isoform 1) | BCAR1, Cas family scaffolding protein | CRK-associated substrate | BCAR1, Cas family scaffold protein | Crk-associated substrate p130Cas | P130Cas

BCAR1: A Non-Coding RNA Molecule as A Potential Drug Target Or Biomarker for Cancer

BCAR1 (Bcl-2-associated RNA 1) is a non-coding RNA molecule that has been identified as a potential drug target or biomarker for various diseases, including cancer. BCAR1 is a key regulator of the Bcl-2 gene, which is a well-known tumor suppressor gene that plays a crucial role in preventing the development and progression of cancer.

The Bcl-2 gene encodes for a protein that is involved in cell survival and apoptosis, which are critical processes that regulate cell growth and development. The Bcl-2 gene has four splice variants, which generate four different RNA molecules, including BCAR1, BCAR2, BCAR3, and BCAR4.

Studies have shown that BCAR1 is expressed in various tissues and cells, including human tissues, cancer cells, and normal cells. It has also been shown to play a role in various cellular processes, including cell proliferation, apoptosis, and cell survival.

One of the key functions of BCAR1 is its role in the Bcl-2 signaling pathway. The Bcl-2 signaling pathway is a well-established pathway that involves the interaction between the Bcl-2 protein and various downstream targets, including BCAR1. This signaling pathway is involved in the regulation of cell survival and apoptosis, as well as cell cycle progression.

Studies have shown that the Bcl-2 signaling pathway is involved in the development and progression of various diseases, including cancer. Therefore, targeting BCAR1 and its downstream targets may be a promising strategy for the development of new treatments for these diseases.

Another potential mechanism by which BCAR1 may be involved in the development of cancer is its role in the regulation of cell-cell adhesion. Adhesion is a critical process that involves the interaction between cells, including the formation of tight junctions between epithelial cells. The Bcl-2 signaling pathway is involved in the regulation of cell-cell adhesion, and BCAR1 has been shown to play a role in this process.

Studies have shown that BCAR1 is involved in the regulation of cell-cell adhesion in various ways. For example, one study shown that BCAR1 was expressed in the adherens junction, which is a critical structure that separates epithelial cells and forms tight junctions. This suggests that BCAR1 may be involved in the regulation of tight junction formation and maintenance.

In addition to its role in cell-cell adhesion, BCAR1 may also be involved in the regulation of cell apoptosis. Apoptosis is a natural process that involves the programmed cell death that is necessary for the development and progression of cancer. The Bcl-2 signaling pathway is involved in the regulation of cell apoptosis, and BCAR1 has been shown to play a role in this process.

Studies have shown that BCAR1 is involved in the regulation of cell apoptosis in various ways. For example, one study showed that BCAR1 was shown to induce cell apoptosis in cancer cells. This suggests that targeting BCAR1 with drugs that can inhibit its function may be a promising strategy for the treatment of cancer.

Another potential mechanism by which BCAR1 may be involved in the development of cancer is its role in the regulation of cell-cycle progression. The Bcl-2 signaling pathway is involved in the regulation of cell-cycle progression, and BCAR1 has been shown to play a role in this process.

Studies have shown that BCAR1 is involved in the regulation of cell-cycle progression in various ways. For example, one study showed that BCAR1 was shown to promote the G1 phase of the cell cycle in cancer cells. This suggests that targeting BCAR1 with drugs that can inhibit its function may be a promising strategy for the treatment of cancer.

In conclusion, BCAR1 is a non-coding RNA molecule that has been identified as a potential drug target or biomarker for various diseases, including cancer. BCAR1 plays a crucial role in the regulation of cell

Protein Name: BCAR1 Scaffold Protein, Cas Family Member

Functions: Docking protein which plays a central coordinating role for tyrosine kinase-based signaling related to cell adhesion (PubMed:12832404, PubMed:12432078). Implicated in induction of cell migration and cell branching (PubMed:12432078, PubMed:12832404, PubMed:17038317). Involved in the BCAR3-mediated inhibition of TGFB signaling (By similarity)

The "BCAR1 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about BCAR1 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

BCAR3 | BCAR3-AS1 | BCAR4 | BCAS1 | BCAS2 | BCAS2P2 | BCAS3 | BCAS4 | BCAT1 | BCAT2 | BCCIP | BCDIN3D | BCDIN3D-AS1 | BCHE | BCKDHA | BCKDHB | BCKDK | BCL10 | BCL10-AS1 | BCL11A | BCL11B | BCL2 | BCL2A1 | BCL2L1 | BCL2L10 | BCL2L11 | BCL2L12 | BCL2L13 | BCL2L14 | BCL2L15 | BCL2L2 | BCL2L2-PABPN1 | BCL3 | BCL6 | BCL6B | BCL7A | BCL7B | BCL7C | BCL9 | BCL9L | BCLAF1 | BCLAF3 | BCO1 | BCO2 | BCOR | BCORL1 | BCORP1 | BCR | BCR(BACURD1) E3 ubiquitin ligase complex | BCR(BACURD3) E3 ubiquitin ligase complex | BCR(KLHL12) E3 ubiquitin ligase complex | BCR(KLHL20) E3 ubiquitin ligase complex | BCR(KLHL22) E3 ubiquitin ligase complex | BCR(KLHL9-KLHL13) E3 ubiquitin ligase complex | BCRP2 | BCRP3 | BCRP4 | BCRP5 | BCRP6 | BCRP7 | BCS1L | BCYRN1 | BDH1 | BDH2 | BDKRB1 | BDKRB2 | BDNF | BDNF-AS | BDP1 | BEAN1 | BEAN1-AS1 | BECN1 | BECN2 | BEGAIN | BEND2 | BEND3 | BEND3P3 | BEND4 | BEND5 | BEND6 | BEND7 | BEST1 | BEST2 | BEST3 | BEST4 | BET1 | BET1L | beta-Adrenoceptor | beta-Crystallin | beta-Hexosaminidase Complex | beta-Secretase | BEX1 | BEX2 | BEX3 | BEX4 | BEX5 | BFAR | BFSP1 | BFSP2 | BFSP2-AS1