Non-coding RNAs regulate mitochondrial dynamics in the development of gastric cancer
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Published on: June 15, 2018
Xiatian Chen1,2, Chuang Wei1,2, Liting Huang1,2
1Institute of Translational Medicine, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Abstract:
Gastric cancer (GC) is a malignant cancer that reduces life expectancy worldwide. Although treatment strategies have improved, patients with GC still have poor prognoses. Hence, it is necessary to understand the molecular mechanisms of GC and to find new therapeutic targets. Mitochondrial dynamics and mitochondrial dysfunction are associated with cancer cell growth and progression. Numerous studies have reported that non-coding RNAs (ncRNAs) can participate in the occurrence and development of GC by regulating mitochondrial dynamics. Elucidating the crosstalk between ncRNAs and mitochondria would be helpful in preventing and treating GC. Herein, we review and summarize the functions of oncogenes and tumor suppressors in suppressing ncRNAs and regulating mitochondrial dynamics in GC tumor growth, proliferation, invasion and metastasis. This review provides new insights into the pathogenesis of and intervention for GC.
Insights
This review explores how non-coding RNAs (ncRNAs) and mitochondrial dynamics impact gastric cancer (GC) progression. Understanding this relationship offers new therapeutic targets for this deadly disease.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer (GC) remains a leading cause of cancer mortality worldwide, with poor prognoses despite treatment advancements.
- Mitochondrial dynamics and dysfunction are increasingly recognized as critical factors in cancer cell growth and progression.
- Non-coding RNAs (ncRNAs) have emerged as key regulators in various cancers, including GC.
Purpose of the Study:
- To review and summarize the molecular mechanisms underlying gastric cancer (GC) pathogenesis.
- To elucidate the role of non-coding RNAs (ncRNAs) in regulating mitochondrial dynamics in GC.
- To identify potential therapeutic targets by understanding the interplay between ncRNAs, mitochondria, and GC progression.
Main Methods:
- Literature review of studies investigating ncRNAs, mitochondrial dynamics, and gastric cancer.
- Analysis of the functions of oncogenes and tumor suppressors in regulating ncRNAs and mitochondrial dynamics.
- Synthesis of current knowledge on the pathogenesis and therapeutic interventions for GC.
Main Results:
- Non-coding RNAs (ncRNAs) significantly influence gastric cancer (GC) development and progression by modulating mitochondrial dynamics.
- Oncogenes and tumor suppressors play crucial roles in suppressing ncRNAs and altering mitochondrial dynamics, impacting GC tumor growth, invasion, and metastasis.
- The intricate crosstalk between ncRNAs and mitochondria is a key determinant in GC pathogenesis.
Conclusions:
- Elucidating the relationship between ncRNAs and mitochondrial dynamics provides novel insights into gastric cancer (GC) development.
- Targeting the interplay between ncRNAs and mitochondria presents a promising strategy for future GC prevention and treatment.
- This review highlights new avenues for understanding and intervening in GC pathogenesis.
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