Metabolic reprogramming of drug resistance in pancreatic cancer: mechanisms and effects
- Jinyi Zhang 1, Xueqing Kong 1, Boyan Zhou 1, Rui Li 1, Zhaoan Yu 1, Jinrong Zhu 1, Qing Xi 1, Yan Li 1, Zichao Zhao 2, Rongxin Zhang 1
- Jinyi Zhang 1, Xueqing Kong 1, Boyan Zhou 1
- 1Guangdong Provincial Key Laboratory for Biotechnology Drug Candidates, Department of Biotechnology, Laboratory of Immunology and Inflammation, School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou,The Second Clinical Medical School of Guangdong Pharmaceutical University, Guangzhou, China.
- 2Department of Emergency Medicine, Shaodong People's Hospital, Shaodong City, Hunan Province, China.
- 0Guangdong Provincial Key Laboratory for Biotechnology Drug Candidates, Department of Biotechnology, Laboratory of Immunology and Inflammation, School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou,The Second Clinical Medical School of Guangdong Pharmaceutical University, Guangzhou, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Pancreatic cancer
Area Of Science
- Gastrointestinal Oncology
- Cancer Metabolism
- Epigenetics
Background
- Pancreatic cancer is a deadly malignancy with high mortality.
- Late diagnosis and chemoresistance complicate treatment.
- Metabolic reprogramming is crucial for cancer cell growth.
Purpose Of The Study
- To review the link between metabolic reprogramming and chemotherapy resistance in pancreatic cancer.
- To discuss the mechanisms driving these processes.
- To summarize therapeutic strategies targeting cancer metabolism.
Main Methods
- Literature review of preclinical studies.
- Analysis of mechanisms of metabolic reprogramming.
- Summary of drug development targeting metabolic pathways.
Main Results
- Metabolic alterations support pancreatic cancer proliferation and metastasis.
- Epigenetic mechanisms may mediate metabolic changes.
- Targeting metabolism shows promise in preclinical models.
Conclusions
- Metabolic reprogramming is a key driver of pancreatic cancer and chemoresistance.
- Targeting metabolic pathways offers potential therapeutic strategies.
- Further research is needed to translate these findings into clinical practice.
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