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Current status and prospects of GREM1 research in cancer (Review)
Dantong Zhu1, Dong Zhao1, Naixue Wang2
1Department of Medical Oncology, General Hospital of Northern Theater Command, Shenyang, Liaoning 110000, P.R. China.
Abstract:
GREM1 is a secreted protein that antagonizes bone morphogenetic proteins (BMPs) and participates in critical biological processes, including embryonic development, organogenesis and tissue differentiation. Gremlin 1 (GREM1) is also an inhibitor of TGF-β and a ligand for vascular endothelial growth factor receptor 2. In addition, GREM1 can induce cells, participate in the process of epithelial-mesenchymal transition, and then participate in tumor development. GREM1 has a variety of biological functions and can participate in the malignant progression of a variety of tumors through the BMP signaling pathway. GREM1 also can inhibit TGF-β in some tumors, thereby inhibiting tumors, and its involvement in tumor development varies in different types of cancer. The present review examines the role and function of GREM1 in tumors. GREM1 is expressed in a variety of tumor types. GREM1 expression can affect the epithelial-mesenchymal transformation of tumor cells. GREM1 has been studied in breast and colon cancer, and its potential role is to promote cancer. However, in pancreatic cancer, which was found to act differently from other cancer types, overexpression of GREM1 inhibits tumor metastasis. The present review suggests that GREM1 can be a diagnostic and prognostic indicator. In future studies, the study of GREM1 based on single-cell sequencing technology will further clarify its role and function in tumors.
Insights
Gremlin 1 (GREM1) is a protein with varied roles in cancer, promoting some tumors while inhibiting others like pancreatic cancer. Further research using single-cell sequencing may clarify its diagnostic and prognostic potential.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Gremlin 1 (GREM1) is a secreted protein involved in embryonic development and tissue differentiation.
- GREM1 antagonizes bone morphogenetic proteins (BMPs) and inhibits transforming growth factor-beta (TGF-β).
- GREM1 acts as a ligand for vascular endothelial growth factor receptor 2 and influences epithelial-mesenchymal transition.
Purpose of the Study:
- To review the multifaceted role and function of Gremlin 1 (GREM1) in the development and progression of various tumors.
- To explore GREM1's dual function in cancer, acting as a promoter in some and an inhibitor in others.
- To assess GREM1's potential as a diagnostic and prognostic biomarker in oncology.
Main Methods:
- Review of existing literature on Gremlin 1 (GREM1) expression and function in different cancer types.
- Analysis of GREM1's involvement in signaling pathways, including BMP and TGF-β.
- Examination of GREM1's impact on epithelial-mesenchymal transition and tumor metastasis.
Main Results:
- GREM1 is expressed in diverse tumor types and influences epithelial-mesenchymal transformation.
- In breast and colon cancer, GREM1 generally promotes tumor progression.
- Conversely, in pancreatic cancer, GREM1 overexpression inhibits tumor metastasis, indicating context-dependent roles.
Conclusions:
- Gremlin 1 (GREM1) exhibits complex and cancer-specific functions, acting as both an oncogene and a tumor suppressor.
- GREM1 holds promise as a potential diagnostic and prognostic indicator in various malignancies.
- Future studies employing single-cell sequencing technology are crucial for a deeper understanding of GREM1's precise roles in tumors.
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