The potency of Pentagamavunone‐0 (PGV‐0) as chemopreventive agent for the formation and growth of breast cancer as revealed in 3D model
Wulandari Wulandari(1), Muthi’ Ikawati(2), Edy Meiyanto(3*)
(1) Graduate School, Universitas Gadjah Mada, Jl. Teknika Utara, Yogyakarta 55281, Indonesia; Cancer Chemoprevention Research Center, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia
(2) Cancer Chemoprevention Research Center, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia
(3) Cancer Chemoprevention Research Center, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia
(*) Corresponding Author
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Bashari MH, Huda F, Tartila TS, Shabrina S, Putri T, Qomarilla N, Atmaja H, Subhan B, Sudji IR, Meiyanto E. 2019. Bioactive compounds in the ethanol extract of marine sponge Stylissa carteri demonstrates potential anticancer activity in breast cancer cells. Asian Pac J Cancer Prev. 20(4):1199–1206. doi:10.31557/APJCP.2019.20.4.1199.
Boutin ME, Voss TC, Titus SA, CruzGutierrez K, Michael S, Ferrer M. 2018. A highthroughput imaging and nuclear segmentation analysis protocol for cleared 3D culture models. Sci Rep. 8:11135. doi:10.1038/s41598018291690.
Da’i M, Meiyanto E, Supardjan A. 2004. Efek antiproliferatif Pentagamavunon0 terhadap sel myeloma [Antiproliferative effect of Pentagamavunon0 on myeloma cells]. Sains Kesehatan. 17(1):1–11.
Da’i M, Meiyanto E, Supardjan A, Jenie UA, Kawaichi M. 2007. Potensi antiproliferatif analog kurkumin Pentagamavunon terhadap sel kanker payudara T47D [Antiproliferative effects of curcumin analogue Pentagamavunone in T47D breast cancer cells]. Artocarpus. 7(1):14–20.
Da’i M, Suhendi A, Meiyanto E, Jenie UA, Kawaichi M. 2017. Apoptosis induction effect of curcumin and its analogs Pentagamavunon0 and Pentagamavunon1 on cancer cell lines. Asian J Pharm Clin Res. 10(3):373–376. doi:10.22159/ajpcr.2017.v10i3.16311.
Edmondson R, Broglie JJ, Adcock AF, Yang L. 2014. Threedimensional cell culture systems and their applications in drug discovery and cellbased biosensors. Assay Drug Dev Technol. 12(4):207–218. doi:10.1089/adt.2014.573.
Hermawan A, Fitriasari A, Junedi S, Ikawati M, Haryanti S, Widaryanti B, Da’i M, Meiyanto E. 2011. PGV 0 and PGV1 increased apoptosis induction of doxorubicin on MCF7 breast cancer cells. Pharmacon. 12(2):55–59. doi:10.23917/pharmacon.v12i2.32.
Ho WY, Yeap SK, Ho CL, Rahim RA, Alitheen NB. 2012. Development of multicellular tumor spheroid (MCTS) culture from breast cancer cell and a high throughput screening method using the MTT assay. PLoS ONE. 7(9):e44640. doi:10.1371/journal.pone.0044640.
Ikawati M, Purwanto H, Imaniyyati NN, Afifah A, Sagiyo ML, Yohanes J, Sismindari, Ritmaleni. 2018. Cytotoxicity of Tetrahydropentagamavunon0 (THPGV 0) and Tetrahydropentagamavunon1 (THPGV1) in several cancer cell lines. Indones J Pharm. 29(4):179– 187. doi:10.14499/indonesianjpharm29iss4pp179.
Ikawati M, Septisetyani EP. 2018. Pentagamavunone 0 (PGV0), a curcumin analog, enhances cytotoxicity of 5fluorouracil and modulates cell cycle in WiDr colon cancer cells. Indones J Cancer Chemoprev. 9(1):23–31. doi:10.14499/indonesianjcanchemoprev9iss1pp23 31.
Larasati YA, YonedaKato N, Nakamae I, Yokoyama T, Meiyanto E, Kato J. 2018. Curcumin targets multiple enzymes involved in the ROS metabolic pathway to suppress tumor cell growth. Sci Rep. 8:2039. doi:10.1038/s41598018201796.
Liu X, Chu K. 2014. Ecadherin and gastric cancer: cause, consequence, and applications. Biomed Res International. p. e637308. doi:10.1155/2014/637308.
Meiyanto E. 1999. Kurkumin sebagai obat kanker: menelusuri mekanisme aksinya [Curcumin as an antineoplastic agent: the elucidation of its molecular mechanism of action]. Majalah Farmasi Indonesia. 10(4):224–236.
Meiyanto E, Hermawan A, Anindyajati A. 2012. Natural products for cancertargeted therapy: citrus flavonoids as potent chemopreventive agents. Asian Pac J Cancer Prev. 13(2):427–436. doi:10.7314/APJCP.2012.13.2.427.
Meiyanto E, Putri DPP, Susidarti RA, Sardjiman, Fitriasari A, Husnaa U, Purnomo H, Kawaichi M. 2014. Curcumin and its analogues (PGV0 and PGV1) enhance sensitivity of resistant MCF7 cells to doxorubicin through inhibition of HER2 and NFkB activation. Asian Pac J Cancer Prev. 15(1):179–184. doi:10.7314/APJCP.2014.15.1.179.
Mohammadian M, Salami M, Momen S, Alavi F, EmamDjomeh Z, MoosaviMovahedi AA. 2019. Enhancing the aqueous solubility of curcumin at acidic condition through the complexation with whey protein nanofibrils. Food Hydrocoll. 87:902–914. doi:10.1016/j.foodhyd.2018.09.001.
Pistollato F, Iglesias RC, Ruiz R, Aparicio S, Crespo J, Lopez LD, Giampieri F, Battino M. 2017. The use of natural compounds for the targeting and chemoprevention of ovarian cancer. Cancer Lett. 411:191–200. doi:10.1016/j.canlet.2017.09.050.
Sant S, Johnston PA. 2017. The production of 3D tumor spheroids for cancer drug discovery. Drug Discov Today Technol. 23:27–36. doi:10.1016/j.ddtec.2017.03.002.
Septisetyani EP, Ikawati M, Widaryanti B, Meiyanto E. 2008. Apoptosis mediated cytotoxicity of curcumin analogues PGV0 and PGV1 in WiDr cell line. Proceeding of The International Symposium on Molecular Targeted Therapy Yogyakarta: Faculty of Pharmacy Universitas Gadjah Mada. ISBN: 978979 9510761,:p.48–56.
Utomo RY, Putri H, Pudjono, Susidarti RA, Jenie RI, Meiyanto E. 2017. Synthesis and cytotoxic activity of 2,5bis(4boronic acid)benzylidine cyclopentanone on HER2 overexpressedcancer cells. Indones J Pharm. 28(2):74–81. doi:10.14499/indonesianjpharm28iss2pp74.
DOI: https://doi.org/10.22146/ijbiotech.51759
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