Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/519536
Title: Molecular studies on combined effect of zerumbone and cisplatin in hepatocellular carcinoma in vitro and in vivo studies
Researcher: Srimathi Devi, J
Guide(s): Haripriya, D
Keywords: e hepatitis B virus and hepatitis C virus
Engineering
Engineering and Technology
Engineering Biomedical
Hepatocellular carcinoma
Liver cancer
University: Anna University
Completed Date: 2023
Abstract: Liver cancer is the fifth most common cancer and the second most newlinefrequent cause of cancer-related death globally. Hepatocellular carcinoma newlinerepresents about 90% of primary liver cancers and constitutes a major global newlinehealth challenge. Infection by the hepatitis B virus and hepatitis C virus are the newlinemain risk factors for HCC development, although non-alcoholic steatohepatitis newlineassociated with acquired and inherited metabolic syndrome or diabetes newlinemellitus, chronic alcohol abuse, genetic hemochromatosis, and aflatoxin newlineexposure are other frequent risk factors. newlineCisplatin (CIS), cis-diamminedichloroplatinum (II), a well-known newlinechemotherapeutic medication, is currently being used as first-line therapy for newlineovarian, testicular, cervical, head and neck, bladder, breast, brain, and newlinesmall-cell lung cancers, either alone or in combination with other anti-cancer newlinedrugs. Although CIS is recognized for its efficacy in the treatment of a broader newlinerange of cancer types, the development of chemo-resistance and undesirable newlineside effects such as nephrotoxicity, ototoxicity, hepatotoxicity, allergic newlinereactions, impaired immunity to infections, gastrointestinal disorders, and newlinehemorrhage are all unwanted side effects that make CIS unsuitable for many newlinepatients, depriving them of the best and most beneficial effects of newlinechemotherapy. To address these challenges, combining conventional newlinechemotherapeutic medications with natural products is an ideal strategy for newlineincreasing cancer cell sensitivity to treatments and providing synergistic newlineanti-tumor efficacy by avoiding the pathways and biomarkers that cause liver newlinecancer. newline newline
Pagination: xxvii,215p.
URI: http://hdl.handle.net/10603/519536
Appears in Departments:Faculty of Technology

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02_prelim pages.pdf4.15 MBAdobe PDFView/Open
03_contents.pdf140.2 kBAdobe PDFView/Open
04_abstracts.pdf16.27 kBAdobe PDFView/Open
05_chapter1.pdf1.69 MBAdobe PDFView/Open
06_chapter2.pdf409.23 kBAdobe PDFView/Open
07_chapter3.pdf487.72 kBAdobe PDFView/Open
08_chapter4.pdf2.69 MBAdobe PDFView/Open
09_chapter5.pdf466.78 kBAdobe PDFView/Open
10_annexures.pdf222.18 kBAdobe PDFView/Open
80_recommendation.pdf103.83 kBAdobe PDFView/Open
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