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Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer
Yanqin Luo1, Jingyang Li1, Peng Yu1
1State Key Laboratory of Southwestern Chinese Medicine Resources, College of Pharmacy, Innovative Institute of Chinese Medicine and Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, P. R. China.
Abstract:
Lung cancer is a leading cause of cancer-related mortality worldwide, with non-small cell lung cancer (NSCLC) being the most common histological type. Owing to the limited therapeutic efficacy and side effects of currently available therapies for NSCLC, it is necessary to identify novel therapeutic targets for NSCLC. Long non-coding RNAs (lncRNAs) are non-protein-coding RNAs with a transcript length of more than 200 nucleotides, which play a vital role in the tumorigenesis and progression of multiple cancers, including NSCLC. Induction of programmed cell death (PCD) is the main mechanism leading to tumour cell death in most cancer treatments. Recent studies have demonstrated that lncRNAs are closely correlated with PCD including apoptosis, pyroptosis, autophagy and ferroptosis, which can regulate PCD and relevant death pathways to affect NSCLC progression and the efficacy of clinical therapy. Therefore, in this review, we focused on the function of lncRNAs in PCD of NSCLC and summarized the therapeutic role of targeting lncRNAs in PCD for NSCLC treatment, aiming to provide new sights into the underlying pathogenic mechanisms and propose a potential new strategy for NSCLC therapy so as to improve therapeutic outcomes with the ultimate goal to benefit the patients.
Insights
Long non-coding RNAs (lncRNAs) regulate programmed cell death (PCD) in non-small cell lung cancer (NSCLC). Targeting lncRNAs in PCD offers a novel therapeutic strategy to improve NSCLC treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Non-small cell lung cancer (NSCLC) remains a major cause of cancer mortality globally.
- Current NSCLC therapies have limitations in efficacy and side effect profiles, necessitating novel therapeutic targets.
- Long non-coding RNAs (lncRNAs) are implicated in cancer development and progression, including NSCLC.
Purpose of the Study:
- To review the role of lncRNAs in regulating programmed cell death (PCD) pathways in NSCLC.
- To summarize the therapeutic potential of targeting lncRNAs involved in PCD for NSCLC treatment.
- To provide insights into NSCLC pathogenesis and propose new therapeutic strategies.
Main Methods:
- Literature review focusing on lncRNAs and their association with various PCD mechanisms (apoptosis, pyroptosis, autophagy, ferroptosis).
- Analysis of how lncRNAs modulate these PCD pathways in the context of NSCLC progression.
- Examination of studies investigating therapeutic strategies targeting lncRNAs for NSCLC.
Main Results:
- lncRNAs are significantly correlated with multiple PCD pathways, influencing NSCLC cell death and tumor progression.
- Dysregulation of specific lncRNAs can promote or inhibit NSCLC development by affecting PCD.
- Targeting lncRNAs involved in PCD presents a promising avenue for enhancing NSCLC treatment efficacy.
Conclusions:
- lncRNAs play a critical role in governing PCD in NSCLC, impacting disease progression and therapeutic responses.
- Targeting lncRNAs within PCD pathways offers a novel and potentially effective strategy for NSCLC therapy.
- Further research into lncRNA-PCD interactions could lead to improved clinical outcomes for NSCLC patients.
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