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Understanding the role of Apoptosis Inhibitor 5 (Api5) in breast cancer

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dc.contributor.advisor LAHIRI, MAYURIKA en_US
dc.contributor.author KUTTANAMKUZHI, ABHIJITH en_US
dc.date.accessioned 2022-05-02T10:25:08Z
dc.date.available 2022-05-02T10:25:08Z
dc.date.issued 2022-03 en_US
dc.identifier.citation 141 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6789
dc.description.abstract The balance between cell death and cell division is essential for the maintenance of homeostasis in multicellular organisms. Apoptosis, or programmed cell death, plays a vital role in the maintenance of this homeostasis and therefore, is a tightly regulated process. Deregulation of apoptosis can lead to cancer. Apoptosis inhibitor 5 (Api5) is an inhibitor of apoptosis. The molecular mechanism underlying the activation and regulation of Api5 is yet to be thoroughly explored. Api5 has been reported to be associated with several cancers, including ovarian, bladder, and lung cancers. Studies suggest that Api5 can be used as a biomarker for ovarian and bladder cancers. However, the role of Api5 in breast cancer, which reports the highest number of deaths due to cancer, remains unclear. My project focuses on investigating the role of Api5 in breast cancer. In vitro overexpression studies using 3D breast acinar cultures demonstrated that overexpression of Api5 resulted in the transformation of non-tumorigenic breast epithelial cells with increased proliferation and various phenotypic changes. Api5 knockdown affected the tumorigenic potential and associated phenotypes of breast cancer cells. Mechanistically Api5 was shown to activate FGF2 signalling, possibly leading to PDK1-Akt and ERK pathway activation. Interestingly Api5-FGF2 signalling activates PDK1-Akt/ cMYC axis during the early days of acinar morphogenesis, while activation of ERK signalling occurred during the later days. Together this led to elevated proliferation, migration, anchorage-independent growth, protein synthesis and reduced apoptosis, supporting the malignant growth of Api5 overexpressing cells. in silico studies using TCGA and GENT2 database demonstrated that elevated levels of Api5 transcript in breast cancers that was also associated with poor patient survival. This further correlated with histopathological analyses of tumour samples where higher expression of Api5 was observed in breast tumour tissue compared to the adjacent normal tissue, thus suggesting that elevated levels of Api5 might be associated with breast malignancy en_US
dc.description.sponsorship Science and Engineering Research Board (SERB), the Government of India (EMR/2016/001974) Indian Institute of Science Education and Research Pune Core funding. Abhijith Kuttanamkuzhi was funded through the Council of Scientific and Industrial Research (CSIR)-SRF fellowship en_US
dc.language.iso en en_US
dc.subject Indian Breast Cancer en_US
dc.subject Breast cancer en_US
dc.subject Apoptosis en_US
dc.subject Api5 en_US
dc.subject FGF2 en_US
dc.subject Transformation en_US
dc.subject Proliferation en_US
dc.subject Morphogenesis en_US
dc.subject Breast en_US
dc.subject TCGA en_US
dc.title Understanding the role of Apoptosis Inhibitor 5 (Api5) in breast cancer en_US
dc.type Thesis en_US
dc.publisher.department Dept. of Biology en_US
dc.type.degree Ph.D en_US
dc.contributor.department Dept. of Biology en_US
dc.contributor.registration 20163438 en_US


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  • PhD THESES [583]
    Thesis submitted to IISER Pune in partial fulfilment of the requirements for the degree of Doctor of Philosophy

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