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Published on: August 2, 2024
MOB kinase activator 1A acts as an oncogene by targeting PI3K/AKT/mTOR in ovarian cancer
Jian Lei1,2, Jing-Ying Xu1, Min Hu1
1Department of Obstetrics and Gynecology, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, 361003, China.
Background:
To illuminate the precise roles of MOB Kinase Activator 1 A (MOB1A) in the development of ovarian cancer (OC).
Methods:
MOB1A expression and clinical data of OC were obtained from the public database on gene expression and proteomics. Meanwhile, verification of expression was carried out in Gene Expression Omnibus, the Human Protein Atlas, and OC cell lines. The prognosis of MOB1A was explored in the Kaplan-Meier plotter. RNA interference and lentivirus vectors were applied to construct knockdown and overexpressed cell models. Changes in the malignant behaviors of OC cells were detected by cholecystokinin octopeptide cell counting kit, wound healing, colony formation assay, transwell, flow cytometry assays, and in vivo experiments. Changes in proteins in the PI3K and autophagy-related makers were detected by western blot analysis.
Results:
The expression of MOB1A was significantly upregulated and accompanied by an inferior survival rate in OC. Knockdown of MOB1A inhibited the proliferation, invasion, migration, and cell cycle of OC cells, whereas induced cell autophagy. MOB1A upregulation had the opposite effects. In addition, bioinformatics analysis and western blot experiments showed that MOB1A plays an important role in the PI3K/AKT/mTOR pathway.
Conclusions:
Our findings indicated that MOB1A is highly expressed and related to poor prognosis in OC. MOB1A plays a role in promoting the malignant biological behavior of tumor cells through PI3K/AKT/mTOR signaling pathway.
Insights
MOB Kinase Activator 1A (MOB1A) is highly expressed in ovarian cancer (OC), promoting tumor growth and poor survival. Inhibiting MOB1A suppresses OC cell malignancy via the PI3K/AKT/mTOR pathway.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Ovarian cancer (OC) remains a significant health challenge with complex underlying mechanisms.
- Understanding the role of specific genes like MOB Kinase Activator 1A (MOB1A) is crucial for developing targeted therapies.
Purpose of the Study:
- To elucidate the specific functions and implications of MOB1A in the pathogenesis and progression of ovarian cancer.
- To investigate the molecular pathways influenced by MOB1A in OC development.
Main Methods:
- Utilized public databases (gene expression, proteomics) and validation in OC cell lines and datasets.
- Employed RNA interference and lentivirus vectors for MOB1A knockdown and overexpression models.
- Assessed malignant behaviors (proliferation, invasion, migration, cell cycle, autophagy) and PI3K/AKT/mTOR pathway proteins.
Main Results:
- MOB1A expression was significantly upregulated in OC, correlating with poorer patient survival.
- Knockdown of MOB1A inhibited OC cell proliferation, invasion, and migration, while inducing autophagy.
- Conversely, MOB1A upregulation enhanced malignant behaviors; pathway analysis implicated MOB1A in the PI3K/AKT/mTOR signaling.
Conclusions:
- MOB1A is a key driver in ovarian cancer, exhibiting high expression linked to adverse prognosis.
- MOB1A promotes tumor cell malignancy through the PI3K/AKT/mTOR signaling pathway, representing a potential therapeutic target.
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