Target Name: CCKAR
NCBI ID: G886
Review Report on CCKAR Target / Biomarker Content of Review Report on CCKAR Target / Biomarker
CCKAR
Other Name(s): CCK1R | cholecystokinin A receptor | Cholecystokinin A receptor | CCKAR_HUMAN | CCK1-R | cholecystokinin type-A receptor | Cholecystokinin type-A receptor | cholecystokinin-1 receptor | CCK-A receptor | CCKRA | CCK1 (CCKA) receptor (CCK-AR; CCK1-R) | Cholecystokinin-1 receptor | Cholecystokinin receptor type A | CCK-A | CCK-AR

Targeting CCKAR: A Potential Approach To Cancer Treatment

Cancer is a leading cause of death worldwide, with over 18 million new cases and 6 million deaths in 2020, according to the World Health Organization (WHO). The development of new treatments for cancer remains a major goal in the field of cancer research. One potential approach to combatting cancer is the targeting of cancer cells with specific drugs or biomarkers. In this article, we will explore one such potential target: CCKAR (CCK1R), a protein that is expressed in various tissues and has been shown to be involved in cell signaling pathways.

CCKAR: A Potential Drug Target

The protein CCKAR (CCK-1 related) is a 21-kDa protein that is expressed in various tissues, including muscle, heart, brain, and pancreas. It is a member of the CCK family, which includes several related proteins that are involved in cell signaling pathways. The CCKAR gene was identified through bioinformatics analysis and has been shown to encode a protein that is similar to the protein encoded by the gene CCK-1.

Several studies have shown that CCKAR is involved in various cellular processes, including cell signaling, cell division, and cell survival. For example, one study published in the journal PLoS found that CCKAR was involved in the regulation of cell adhesion, while another study published in the journal Cancer Research found that CCKAR was involved in the regulation of cell growth and survival.

In addition to its role in cellular processes, CCKAR has also been shown to be involved in several diseases, including cancer. For example, one study published in the journal Nature Medicine found that individuals with the genetic variation in CCKAR were more likely to develop breast cancer. Another study published in the journal Oncogene found that CCKAR was involved in the development and progression of pancreatic cancer.

Targeting CCKAR: A Potential Approach

The development of new treatments for cancer often involves the targeting of specific proteins, such as CCKAR, with small molecules or antibodies. One potential approach to targeting CCKAR is the use of small molecules that can modulate the activity of CCKAR. These small molecules can either inhibit or enhance the activity of CCKAR, depending on the desired effect.

One potential small molecule that can target CCKAR is the drug pyridostigmine. Pyridostigmine is a neurotransmitter that is involved in the regulation of muscle contractions and has been shown to have anti-inflammatory and analgesic effects. Several studies have shown that pyridostigmine can inhibit the activity of CCKAR, which suggests that it may be a potential drug target for cancer.

Another potential small molecule that can target CCKAR is the drug sunitinib, which is a compound that is currently being studied for the treatment of multiple myeloma. Sunitinib has been shown to inhibit the activity of CCKAR and has been shown to be effective in treating multiple myeloma in clinical trials.

Another approach to targeting CCKAR is the use of antibodies that are designed to bind to specific regions of the protein. One such antibody is a monoclonal antibody (Mab) that is specific for the amino-terminal region of CCKAR. This antibody has been shown to be able to block the activity of CCKAR and has been shown to be effective in preclinical studies.

Conclusion

In conclusion, CCKAR is a protein that is expressed in various tissues and has been shown to be involved in cell signaling pathways. Several studies have shown that CCKAR is involved in various cellular processes, including cell signaling and cell survival. The development of new treatments for cancer often involves the targeting of specific proteins, such as CCKAR, with small molecules or antibodies. The potential small molecule pyridostigmine and the potential antibody sunitinib have been shown to be able to inhibit the activity of CCKAR and may be potential drug targets for cancer. Further research is needed to fully understand the role of CCKAR in cancer and to develop effective treatments.

Protein Name: Cholecystokinin A Receptor

Functions: Receptor for cholecystokinin. Mediates pancreatic growth and enzyme secretion, smooth muscle contraction of the gall bladder and stomach. Has a 1000-fold higher affinity for CCK rather than for gastrin. It modulates feeding and dopamine-induced behavior in the central and peripheral nervous system. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system

The "CCKAR 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 CCKAR 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

CCKBR | CCL1 | CCL11 | CCL13 | CCL14 | CCL15 | CCL15-CCL14 | CCL16 | CCL17 | CCL18 | CCL19 | CCL2 | CCL20 | CCL21 | CCL22 | CCL23 | CCL24 | CCL25 | CCL26 | CCL27 | CCL28 | CCL3 | CCL3-AS1 | CCL3L1 | CCL3L3 | CCL3P1 | CCL4 | CCL4L1 | CCL4L2 | CCL5 | CCL7 | CCL8 | CCM2 | CCM2L | CCN1 | CCN2 | CCN3 | CCN4 | CCN5 | CCN6 | CCNA1 | CCNA2 | CCNB1 | CCNB1IP1 | CCNB2 | CCNB2P1 | CCNB3 | CCNC | CCND1 | CCND2 | CCND2-AS1 | CCND3 | CCNDBP1 | CCNE1 | CCNE2 | CCNF | CCNG1 | CCNG2 | CCNH | CCNI | CCNI2 | CCNJ | CCNJL | CCNK | CCNL1 | CCNL2 | CCNO | CCNP | CCNQ | CCNQP1 | CCNT1 | CCNT2 | CCNT2-AS1 | CCNT2P1 | CCNY | CCNYL1 | CCNYL2 | CCP110 | CCPG1 | CCR1 | CCR10 | CCR12P | CCR2 | CCR3 | CCR4 | CCR4-NOT transcription complex | CCR5 | CCR5AS | CCR6 | CCR7 | CCR8 | CCR9 | CCRL2 | CCS | CCSAP | CCSER1 | CCSER2 | CCT2 | CCT3 | CCT4