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Influence of inherent tissue mechanics and cellular heterogeneity on epithelial defence against cancer

Implementing Organization

Indian Institute of Science
Principal Investigator
Dr. Medhavi Vishwakarma
Indian Institute of Science

About

Epithelial Defence against Cancer (EDAC) is a defense mechanism in epithelia that eliminates oncogenic cells through cell competition. However, EDAC is impaired when oncogenic cells become fitter than the host, leading to cancer initiation. Aging is a pro-tumorigenic state and is the single most important risk factor for cancer development in epithelial tissues. This project aims to understand how EDAC is impaired as tissue ages, hypothesizing that ageing phenotypes, such as increased transcriptional noise and changing tissue mechanics, might act as regulating factors for epithelial defense against cancer. Using mammary breast epithelia as a model system, the researchers will study tissue heterogeneity as a regulator of EDAC. They will measure biochemical heterogeneity in 2D cultures of MCF10a cells and physical heterogeneity using techniques like live confocal microscopy, real-time PCR, immunostaining, and flow cytometry. They will transform healthy cells into fluorescently tagged oncogenic mutants overexpressing ErbB2, which will influence the fate of oncogenic mutants. The researchers aim to mimic ageing by overexpressing integrin b3 and reducing cell-cell adhesions, modulating tissue mechanics. This study will provide insight into why aged epithelial tissue might be more vulnerable to cancer and help identify treatment strategies exploiting host defense mechanisms against cancer.
Funding Organization
Funding Organization
Science and Engineering Research Board (SERB), New Delhi
Anusandhan National Research Foundation (ANRF)
Quick Information
Area of Research
Life Sciences & Biotechnology
Start Year
2022
End Year
2024
Sanction Amount
₹ 32.14 L
Status
Completed
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
N/A
Startup (If Any)
00
No. of Patents
Filed :00
Grant :00
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