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c-Kit Receptors as a Therapeutic Target in Cancer: Current Insights
Mona S Abdellateif1, Ahmed K Bayoumi2,3, Mohammed Aly Mohammed1
1Medical Biochemistry and Molecular Biology, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, 11796, Egypt.
Abstract:
c-Kit is a type III receptor tyrosine kinase (RTK) that has an essential role in various biological functions including gametogenesis, melanogenesis, hematopoiesis, cell survival, and apoptosis. c-KIT aberrations, either overexpression or loss-of-function mutations, have been implicated in the pathogenesis and development of many cancers, including gastrointestinal stromal tumors, mastocytosis, acute myeloid leukemia, breast, thyroid, and colorectal cancer, making c-KIT an attractive molecular target for the treatment of cancers. Therefore, a lot of effort has been put into investigating the utility of tyrosine kinase inhibitors for the management of c-KIT mutated tumors. This review of the literature illustrates the role of c-KIT mutations in many cancers, aiming to provide insights into the role of TKIs as a therapeutic option for cancer patients with c-KIT aberrations. In conclusion, c-KIT is implicated in different types of cancer, and it could be a successful molecular target; however, proper detection of the underlying mutation type is required before starting the appropriate personalized therapy.
Insights
c-Kit receptor tyrosine kinase (RTK) aberrations drive various cancers. Tyrosine kinase inhibitors (TKIs) show promise for treating c-KIT mutated tumors, but precise mutation detection is crucial for personalized therapy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- c-Kit, a type III receptor tyrosine kinase (RTK), regulates critical biological processes like cell survival and apoptosis.
- Aberrations in c-KIT, including overexpression and mutations, are linked to the development of numerous cancers such as gastrointestinal stromal tumors and acute myeloid leukemia.
- The critical role of c-KIT in cancer pathogenesis positions it as a significant molecular target for therapeutic intervention.
Purpose of the Study:
- To review the literature on the role of c-KIT mutations in various cancers.
- To explore the potential of tyrosine kinase inhibitors (TKIs) in managing cancers with c-KIT aberrations.
- To provide insights into c-KIT as a therapeutic target for personalized cancer treatment.
Main Methods:
- Literature review of studies investigating c-KIT mutations and their role in cancer.
- Analysis of research on the efficacy of tyrosine kinase inhibitors (TKIs) in treating c-KIT-driven malignancies.
- Synthesis of findings to evaluate c-KIT as a molecular target.
Main Results:
- c-KIT mutations are implicated in the pathogenesis of diverse cancers, including gastrointestinal stromal tumors, mastocytosis, acute myeloid leukemia, breast, thyroid, and colorectal cancer.
- Tyrosine kinase inhibitors (TKIs) represent a promising therapeutic strategy for cancers harboring c-KIT aberrations.
- The effectiveness of TKIs is dependent on the specific type of c-KIT mutation present.
Conclusions:
- c-KIT plays a significant role in various cancer types, making it a viable molecular target.
- Personalized therapy targeting c-KIT requires accurate detection of the specific underlying mutation.
- TKIs offer a potential avenue for effective cancer treatment in patients with c-KIT aberrations, underscoring the importance of targeted approaches.
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