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RBM5 reduces small cell lung cancer growth, increases cisplatin sensitivity and regulates key
Julie J Loiselle1, Justin G Roy2, Leslie C Sutherland3
1Biomolecular Sciences Program, Laurentian University, Sudbury, ON P3E 2C6, Canada.
Heliyon
|December 14, 2016
Summary
Re-expressing the RBM5 tumor suppressor gene in small cell lung cancer (SCLC) cells slowed growth and increased chemotherapy sensitivity. This highlights RBM5
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Small cell lung cancer (SCLC) is highly aggressive with poor prognosis.
- The tumor suppressor gene RBM5 is downregulated in many cancers, but its role in SCLC is unclear.
Purpose of the Study:
- To investigate the function of RBM5 in SCLC.
- To determine the effects of RBM5 re-expression on SCLC cell lines and patient specimens.
Main Methods:
- Utilized SCLC cell line (GLC20) with RBM5 deletion to create stable RBM5-expressing sublines.
- Performed transcriptome and target identification studies.
- Conducted RNA sequencing on paired SCLC patient tumor and non-tumor samples.
- Performed functional studies on cell growth and chemosensitivity.
Main Results:
- RBM5 re-expression regulated cell cycle and apoptosis in SCLC cells.
- RBM5 significantly downregulated angiogenesis and cell adhesion pathways.
- Decreased RBM5 expression was observed in SCLC patient tumors, correlating with pathway alterations seen in cell lines.
- RBM5 expression slowed SCLC cell growth and enhanced cisplatin sensitivity.
Conclusions:
- RBM5 plays a crucial role in maintaining the non-transformed state of lung cells.
- RBM5 deletion contributes to SCLC development and progression.
- RBM5 re-expression represents a potential therapeutic strategy for SCLC.
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