TY - JOUR
T1 - Expression of key apoptotic genes in hepatocellular carcinoma cell line treated with etoposide-loaded graphene oxide
AU - Gholami, Ahmad
AU - Emadi, Fatemeh
AU - Nazem, Maryam
AU - Aghayi, Roghayeh
AU - Khalvati, Bahman
AU - Amini, Abbas
AU - Ghasemi, Younes
PY - 2020
Y1 - 2020
N2 - Etoposide (Et) is an antineoplastic agent used for cancer treatment as it promotes the apoptosis of cancer cells. One of the important concerns about Et is the poor water solubility and bioavailability which lowers its cytotoxicity for pharmaceutical applications. Here, Et was loaded on a new carrier, made of carboxylated graphene oxide (GO-COOH), to improve the cytotoxicity of Et on hepatocellular carcinoma (Hep-G2) cells without any destruction on the apoptosis pathway of Et. SEM, TEM, UV–Vis, FT-IR, DLS and Raman were utilized as the characterization techniques. The cytotoxicity of Et on Hep-G2 cells was probed by MTT before and after loading on GO-COOH as well as the flow cytometry. Real-time PCR was used to find the expression of apoptotic genes in Hep-G2 cells treated with free Et and Et-loaded GO-COOH (Et-GO-COOH). From MTT results, IC50s of Et and EtGO-COOH were measured as 6 ± 1.73 and 4 ± 0.11 μg/mL, respectively. Real-time PCR results revealed that both Et-GO-COOH and Et caused toxicity through induction of the expression of same seven apoptotic genes. However, Et-GO-COOH acted more efficiently than Et to induce apoptosis in Hep-G2 cells. The findings verified that GO-COOH improved the cytotoxicity effect of Et with no impact on the Et apoptosis pathway.
AB - Etoposide (Et) is an antineoplastic agent used for cancer treatment as it promotes the apoptosis of cancer cells. One of the important concerns about Et is the poor water solubility and bioavailability which lowers its cytotoxicity for pharmaceutical applications. Here, Et was loaded on a new carrier, made of carboxylated graphene oxide (GO-COOH), to improve the cytotoxicity of Et on hepatocellular carcinoma (Hep-G2) cells without any destruction on the apoptosis pathway of Et. SEM, TEM, UV–Vis, FT-IR, DLS and Raman were utilized as the characterization techniques. The cytotoxicity of Et on Hep-G2 cells was probed by MTT before and after loading on GO-COOH as well as the flow cytometry. Real-time PCR was used to find the expression of apoptotic genes in Hep-G2 cells treated with free Et and Et-loaded GO-COOH (Et-GO-COOH). From MTT results, IC50s of Et and EtGO-COOH were measured as 6 ± 1.73 and 4 ± 0.11 μg/mL, respectively. Real-time PCR results revealed that both Et-GO-COOH and Et caused toxicity through induction of the expression of same seven apoptotic genes. However, Et-GO-COOH acted more efficiently than Et to induce apoptosis in Hep-G2 cells. The findings verified that GO-COOH improved the cytotoxicity effect of Et with no impact on the Et apoptosis pathway.
KW - apoptosis
KW - gene expression
KW - graphene oxide
KW - necrosis
UR - https://hdl.handle.net/1959.7/uws:56602
U2 - 10.1016/j.jddst.2020.101725
DO - 10.1016/j.jddst.2020.101725
M3 - Article
SN - 1773-2247
VL - 57
JO - Journal of Drug Delivery Science and Technology
JF - Journal of Drug Delivery Science and Technology
M1 - 101725
ER -