Abstract
Cisplatin is a chemotherapy drug that is widely used as anticancer drug. Cisplatin increases cytotoxicity by interfering with DNA replication and transcription mechanism. Platinum compounds damage tumours via induction of apoptosis, which is mediated by the activation of various signal transduction pathways such as first inducing reactive oxygen species (ROS), interrupting DNA damage and disrupting calcium signalling in and out of cell. Breast cancer cell lines MCF-7, MDA-MB-231 and MDA-MB-468 were selected and cultured then treated with cisplatin to investigate whether different types of cancer cells give different effect. MTT assay is currently the most extensively used method for IC50 measurements. Here, we used MTT to determine the percentage of cell viability after treated with anticancer agent. The value of IC50 of cisplatin for MCF-7 cell lines after 24 hours is 210.14µg/ml. The value of IC50 of cisplatin for MDA-MB-468 after 24 hours is 232.60µg/ml. MDA-MB-231 have the highest IC50 value which 237.58µg/ml compared to both cell lines. The results obtained highlight the differences between the IC50 for each type of cells. We can conclude that cisplatin reduces cell viability and proliferation in breast cancer cells MCF-7, MDA-MB-231 and MDA-MB-468 cultured for 24 hours.
Metadata
| Item Type: | Student Project |
|---|---|
| Creators: | Creators Email / ID Num. Shamsudin, Mohammad Farizul UNSPECIFIED |
| Contributors: | Contribution Name Email / ID Num. Thesis advisor Abd Latip, Normala UNSPECIFIED |
| Subjects: | A General Works > Indexes (General) R Medicine > RC Internal Medicine > Cancer |
| Divisions: | Universiti Teknologi MARA, Selangor > Puncak Alam Campus > Faculty of Pharmacy |
| Programme: | Bachelor of Pharmacy |
| Keywords: | Cisplatin treatment, Breast cancer cell lines, MCF-7, MDA-MB-231, MDA-MB-468 |
| Date: | 2017 |
| URI: | https://ir.uitm.edu.my/id/eprint/123497 |
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