Progress and current status of molecule-targeted therapy and drug resistance in gastric cancer
Abstract:
Gastric cancer is one of the most common malignant tumors in the world. In China, its morbidity and mortality are second only to lung cancer. Chemotherapy combined with targeted therapy brings survival benefits to patients with advanced gastric cancer. Targets for targeted therapy of gastric cancer include human epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), vascular endothelial growth factor (VEGF), mammalian target of rapamycin (mTOR) and Claudin 18.2 (CLDN 18.2). The main challenge of tumor molecule-targeted drugs is resistance. The main mechanisms of drug resistance include tumor establishment of compensatory signaling pathways, target protein changes, tumor microenvironment changes, tumor heterogeneity and tumor adaptation to targeted drugs. The combined action of multiple drug resistance mechanisms promotes the development of targeted drug resistance. In order to attract the attention of researchers, this paper reviews the mechanisms of drug resistance in gastric cancer-targeted therapy. In addition, the research status of drug resistance in molecule-targeted therapy of gastric cancer is summarized. It is of great clinical significance to explore the drug resistance mechanisms of targeted drugs and reverse drug resistance in gastric cancer. Last, the future development of molecule-targeted therapy is prospected.
Insights
Targeted therapy offers survival benefits for advanced gastric cancer patients, but drug resistance remains a significant challenge. This review explores the complex mechanisms driving resistance and discusses future directions for overcoming it.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Gastric cancer is a leading cause of cancer mortality globally, particularly in China.
- Targeted therapies, including those against EGFR, HER2, VEGF, mTOR, and CLDN 18.2, improve outcomes for advanced gastric cancer.
- Drug resistance is a major obstacle in the efficacy of targeted therapies for gastric cancer.
Purpose of the Study:
- To review the mechanisms of drug resistance in gastric cancer targeted therapy.
- To summarize the current research status of drug resistance in molecular targeted therapy for gastric cancer.
- To highlight the clinical significance of understanding and overcoming targeted drug resistance.
Main Methods:
- Literature review of mechanisms of drug resistance in gastric cancer targeted therapy.
- Summary of current research on drug resistance in molecular targeted therapy.
- Exploration of future prospects for targeted therapy in gastric cancer.
Main Results:
- Key resistance mechanisms include compensatory signaling pathways, target protein alterations, tumor microenvironment changes, heterogeneity, and drug adaptation.
- The interplay of multiple resistance mechanisms accelerates the development of targeted drug resistance.
- Understanding these mechanisms is crucial for developing strategies to reverse resistance.
Conclusions:
- Overcoming drug resistance is critical for improving long-term patient survival in gastric cancer.
- Further research into resistance mechanisms and novel therapeutic strategies is warranted.
- Future developments in molecular targeted therapy hold promise for overcoming resistance and enhancing treatment efficacy.
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