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Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
Published on: June 9, 2023
SHMT2 promotes tumor growth through VEGF and MAPK signaling pathway in breast cancer
Shuang-Yan Xie1,2, Ding-Bo Shi3, Yi Ouyang1
1Department of Radiotherapy, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Collaborative Innovation Center for Cancer Medicine 651 Dongfeng Road East, Guangzhou 510060, Guangdong, China.
Abstract:
Cancer cells modulate their metabolic activities to adapt to their growth and proliferation. Despite advances in breast cancer biology having led to the widespread use of molecular targeted therapy and hormonal drugs, the molecular mechanisms in metabolism related to the regulation of breast cancer cell proliferation are still poorly understood. Here, we investigate the possible role of SHMT2, a key enzyme in serine metabolism, in breast cancer. Firstly, SHMT2 is found highly expressed in both breast cancer cells and tissues, and patients with high expression of SHMT2 have a worse prognosis. Moreover, the intervention of SHMT2 by either knockdown or over-expression in vitro induces the effect on breast cancer proliferation. Mechanistically, RNA-seq shows that over-expression of SHMT2 affect multiple signaling pathways and biological process in breast cancer cells. Furthermore, we confirm that SHMT2 promotes breast cancer cell growth through MAPK and VEGF signaling pathways. Finally, we verify the role of SHMT2 in promoting breast cancer growth in the xenograft tumor model. Our results indicate that SHMT2 plays a critical role in regulating breast cancer growth through MAPK, and VEGF signaling pathways, and maybe serve as a therapeutic target for breast cancer therapy.
Insights
Serine hydroxymethyltransferase 2 (SHMT2) is highly expressed in breast cancer, promoting cell proliferation. Targeting SHMT2 may offer a new therapeutic strategy for breast cancer treatment.
Area of Science:
- Biochemistry
- Oncology
- Molecular Biology
Background:
- Breast cancer cell proliferation is linked to metabolic adaptations.
- Molecular mechanisms regulating breast cancer metabolism remain incompletely understood.
- Serine metabolism's role in breast cancer requires further investigation.
Purpose of the Study:
- To investigate the role of serine hydroxymethyltransferase 2 (SHMT2) in breast cancer proliferation.
- To explore SHMT2 as a potential therapeutic target for breast cancer.
Main Methods:
- Analysis of SHMT2 expression in breast cancer cells and tissues.
- In vitro studies involving SHMT2 knockdown and overexpression.
- RNA sequencing (RNA-seq) to identify affected signaling pathways.
- In vivo validation using a xenograft tumor model.
Main Results:
- SHMT2 is highly expressed in breast cancer tissues and cells, correlating with poor prognosis.
- Modulating SHMT2 levels impacts breast cancer cell proliferation in vitro.
- SHMT2 overexpression affects multiple signaling pathways, including MAPK and VEGF.
- SHMT2 promotes tumor growth in vivo via MAPK and VEGF signaling.
Conclusions:
- SHMT2 plays a critical role in breast cancer cell proliferation and growth.
- SHMT2 regulates breast cancer progression through MAPK and VEGF signaling pathways.
- SHMT2 represents a potential therapeutic target for breast cancer treatment.
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