Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/392946
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dc.date.accessioned2022-07-19T04:49:53Z-
dc.date.available2022-07-19T04:49:53Z-
dc.identifier.urihttp://hdl.handle.net/10603/392946-
dc.description.abstractOne of the approaches to treat metastatic cancers is to prevent metastasis by investigating molecular and cellular mechanisms of malignancy. In general cancer cell metastasis comprises of an orderly sequence of pathological molecular events, collectively termed as metastatic cascade; starting with epithelial-mesenchymal transition (EMT); extracellular matrix (ECM) remodeling; intravasation; survival of cancer cells in the blood stream; extravasation and colonization to prosper in a new more cozy environment. EMT is the prime process responsible for modification in cellular characteristics of cancer cells from epithelial to mesenchymal phenotype and triggering ECM remodeling via activation of different proteases such as matrix metalloproteinases (MMPs) to facilitate anoikis resistance, augmented invasiveness and migratory potential to promote metastasis. Triple Negative Breast Cancer (TNBC) is the molecular subtype of breast cancer which constitutes about 10% to 20% of all breast cancer cases. Absence of ER, PR and HER2 receptors on cancer cells is the molecular hallmark of TNBCs. In the early stage, TNBCs well respond to chemotherapy however, the risk of distant metastasis and relapse is always high with poorer prognosis compared to other breast cancer types. The molecular features of TNBC like absence of ER, PR and HER2 receptors and heterogenic cancer cell population, render them unattainable and hence no targeted therapy has been approved yet. Thus there is an urgent need to improve the therapeutic outcomes of TNBC patients by focusing on numerous studies investigating the association of molecular characteristics with this subtype, therapeutic responses and identification of new targets newlineThe aim of the present study was to investigate molecular and cellular mechanisms to establish the therapeutic value of Enterolactone (EL), a mammalian lignan derived from the flax lignan as a potential anti-cancer and anti-metastatic molecule in triple negative breast cancer (TNBC).
dc.format.extentAll Pages
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleExploring Anti metastatic Breast Cancer Potential of Enterolactone a Mammalian Lignan derived from Flax Lignan
dc.title.alternative
dc.creator.researcherMali, Aniket Vijay
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmaceutical biotechnology
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.description.note
dc.contributor.guideKadam, Shivajirao and Co-Guide Hegde M. V.
dc.publisher.placePune
dc.publisher.universityBharati Vidyapeeth Deemed University
dc.publisher.institutionFaculty of Pharmaceutical Sciences
dc.date.registered2012
dc.date.completed2018
dc.date.awarded2018
dc.format.dimensionsAll
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Pharmaceutical Sciences

Files in This Item:
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01_title page thesis.pdfAttached File701.2 kBAdobe PDFView/Open
02_declaration by researcher.pdf743.26 kBAdobe PDFView/Open
03_certificate of guide, research center.pdf2.13 MBAdobe PDFView/Open
04_acknowledgement.pdf114.51 kBAdobe PDFView/Open
05_contents.pdf291.22 kBAdobe PDFView/Open
06_list of tables, graphs & abbreviations.pdf322.01 kBAdobe PDFView/Open
07_abstract.pdf372.77 kBAdobe PDFView/Open
08_chapter 1.pdf1.45 MBAdobe PDFView/Open
09_chapter 2.pdf1.59 MBAdobe PDFView/Open
10_chapter 3.pdf439.46 kBAdobe PDFView/Open
11_chapter 4.pdf1.65 MBAdobe PDFView/Open
12_chapter 5.pdf1.91 MBAdobe PDFView/Open
13_conclusion.pdf358.87 kBAdobe PDFView/Open
14_summary.pdf74.5 kBAdobe PDFView/Open
15_bibliography.pdf538.3 kBAdobe PDFView/Open
80_recommendation.pdf165.28 kBAdobe PDFView/Open


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