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dc.contributor.advisorHiss, Donavon
dc.contributor.advisorGerber, Tonie
dc.contributor.authorAbrahams, Beynon
dc.date.accessioned2021-02-24T12:33:04Z
dc.date.available2022-02-24T22:10:03Z
dc.date.issued2020
dc.identifier.urihttp://hdl.handle.net/11394/7881
dc.descriptionPhilosophiae Doctor - PhDen_US
dc.description.abstractGlobally, breast cancer is the most common cancer affecting women and it is predicted that in 2030 about 12 million deaths will occur with approximately 21.7 million new cases [2]. Genetic risk factors as well as race and ethnicity, account for about 5-10% of all breast cancer occurrences. Triple negative breast cancer (TNBC), tumors that tested negative for oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2), contribute to 10-20% of all breast carcinomas [3,4] and is known to be a more aggressive type of cancer with varying degree of response to chemotherapeutic and radiation therapy [5,6]en_US
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.subjectBreast canceren_US
dc.subjectMCF-7 breast carcinoma cellsen_US
dc.subjectMDA-MB-231 TNBC cellsen_US
dc.subjectTyrosine kinase inhibitoren_US
dc.subjectEGFR inhibitoren_US
dc.titleThe effects of various combinations of different Cdasses of anticancer drugs and tyrosine kinase inhibitors on the human MCF-7 and triple-negative MDA-MB 231 breast carcinoma cell linesen_US
dc.rights.holderUniversity of the Western Capeen_US


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