Cytotoxic Activity of Methoxy-4’amino Chalcone Derivatives Against Leukemia Cell Lines
Penulis/Author
ARINA NOVILLA (1); Prof. Dr. Mustofa, Apt., M.Kes. (2); Dr. Med. dr. Indwiani Astuti (3); Prof. Drs. Jumina, Ph.D. (4); HERY SUWITO (5)
Tanggal/Date
2019
Kata Kunci/Keyword
Abstrak/Abstract
Background: Chemotherapy is a common treatment for leukemia as well as in other cancer treatment. The lack of tumor
selectivity and development of multi-drug resistance by chemotherapy caused the development of new strategy in cancer
treatment become a pressing need. This study was performed to evaluate the anticancer activity and selectivity of seven
derivatives of chalcones against K562 and HL-60 leukemia cell lines.
Materials and Methods: The cytotoxicity of chalcone’s seven derivatives (compound 1-7) was tested by using
3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxyme-thoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) method. The
percentage of cell mortality data was calculated then the IC50 was analyzed using probit analysis (SPSS 17). The selectivity
index (SI) then calculated from IC50 ratio of normal lymphocyte cells and cancerous cells line (HL-60 and K562).
Results: The IC50 of almost all seven tested compounds were lower in HL-60 cell lines (ranged from 1.57 to 9.63 µg/mL) than
K562 cell lines (ranged from 5.87 to 52.56 µg/mL), except for Compound 7 (5.87±0.15 µg/mL). The number and position of
methoxy groups in chalcone derivatives influenced the anticancer and cancer selectivity of chalcone derivatives.
Conclusion: The results revealed that the number and position of methoxy groups in chalcone derivatives influenced the
anticancer and cancer selectivity of chalcone derivatives.
Rumpun Ilmu
Ilmu Kedokteran Dasar & Biomedis
Bahasa Asli/Original Language
English
Level
Nasional
Status
Dokumen Karya
No
Judul
Tipe Dokumen
Aksi
1
47_Cytotoxic activity of methoxy-4’amino chalcone derivatives against leukemia cell lines .pdf
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2
Cytotoxic Activity of Methoxy-4’amino Chalcone Derivatives Against Leukemia Cell Lines (1).pdf