Long Non-Coding RNAs in Drug Resistance of Gastric Cancer: Complex Mechanisms and Potential Clinical Applications.
Xiang-Yu MengXiao BaiAngting KeKaiqiang LiYun LeiSiqi DingDongqiu DaiPublished in: Biomolecules (2024)
Gastric cancer (GC) ranks as the third most prevalent malignancy and a leading cause of cancer-related mortality worldwide. However, the majority of patients with GC are diagnosed at an advanced stage, highlighting the urgent need for effective perioperative and postoperative chemotherapy to prevent relapse and metastasis. The current treatment strategies have limited overall efficacy because of intrinsic or acquired drug resistance. Recent evidence suggests that dysregulated long non-coding RNAs (lncRNAs) play a significant role in mediating drug resistance in GC. Therefore, there is an imperative to explore novel molecular mechanisms underlying drug resistance in order to overcome this challenging issue. With advancements in deep transcriptome sequencing technology, lncRNAs-once considered transcriptional noise-have garnered widespread attention as potential regulators of carcinogenesis, including tumor cell proliferation, metastasis, and sensitivity to chemo- or radiotherapy through multiple regulatory mechanisms. In light of these findings, we aim to review the mechanisms by which lncRNAs contribute to drug therapy resistance in GC with the goal of providing new insights and breakthroughs toward overcoming this formidable obstacle.
Keyphrases
- long non coding rna
- poor prognosis
- cell proliferation
- locally advanced
- transcription factor
- gas chromatography
- patients undergoing
- gene expression
- single cell
- network analysis
- radiation therapy
- early stage
- genome wide identification
- rna seq
- cardiac surgery
- working memory
- photodynamic therapy
- squamous cell carcinoma
- emergency department
- genome wide analysis
- cell cycle
- cardiovascular events
- human health
- stem cells
- radiation induced
- genome wide
- cardiovascular disease
- acute kidney injury
- free survival
- rectal cancer
- tandem mass spectrometry
- combination therapy
- bone marrow
- pi k akt
- heat shock protein