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A Mass Spectrometry-Based Approach to Identify Phosphoprotein Phosphatases and their Interactors
Published on: April 29, 2022
Measles virus phosphoprotein inhibits apoptosis and enhances clonogenic and migratory properties in HeLa cells
Sankhajit Bhattacharjee1, Rishi Kumar Jaiswal, Pramod Kumar Yadava
1Applied Molecular Biology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi 110 067, India.
Abstract:
Measles virus is the causative agent of measles, a major cause of child mortality in developing countries. Two major proteins, coded by the viral genome, are nucleocapsid protein (N) and phosphoprotein (P). The N protein protects the viral genomic RNA and forms ribonucleoprotein complex (RNP) together with P protein. MeV-P protein recruits the large protein (L), i.e. viral RNA-depended RNA polymerase (RdRp), to ensure viral replication in host cell. Apoptogenic properties of N protein of Edmonston vaccine strain have been established in our lab previously. We investigated the role of MeV-P protein of Edmonston vaccine strain as modulator of apoptosis in cervical cancer cell line (HeLa) and found that MeV-P protein is anti-apoptotic and enhances cell proliferation. Measles virus is considered to be innately oncotropic virus. However, the anti-apoptotic property of MeV-P protein raises important concerns while adopting this virus as an anti-cancer therapeutic tool.
Insights
Measles virus phosphoprotein (P) from the Edmonston strain was found to be anti-apoptotic in HeLa cervical cancer cells, promoting cell proliferation. This finding raises concerns for using measles virus as an oncotropic cancer therapy.
Area of Science:
- Virology
- Molecular Biology
- Cancer Research
Background:
- Measles virus (MeV) causes significant child mortality globally.
- Key viral proteins include nucleocapsid (N) and phosphoprotein (P).
- MeV is considered an oncotropic virus with potential therapeutic applications.
Purpose of the Study:
- To investigate the role of MeV phosphoprotein (P) from the Edmonston vaccine strain.
- To determine MeV-P's function as a modulator of apoptosis in HeLa cervical cancer cells.
Main Methods:
- Cell culture of HeLa cervical cancer cells.
- Analysis of apoptosis modulation by MeV-P protein.
- Assessment of cell proliferation enhancement by MeV-P.
Main Results:
- MeV-P protein exhibits anti-apoptotic properties in HeLa cells.
- MeV-P enhances the proliferation of cervical cancer cells.
- The anti-apoptotic function of MeV-P impacts its therapeutic potential.
Conclusions:
- MeV-P protein possesses anti-apoptotic and cell proliferation-enhancing activities.
- These properties of MeV-P warrant careful consideration for measles virus-based cancer therapy.
- Further research is needed to understand the implications of MeV-P's function in oncotropism.
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