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Identification of Nrf2/STAT3 axis in induction of apoptosis through sub‐G 1 cell cycle arrest mechanism in HT‐29 colon cancer cells

We investigated the role of stattic as an adjuvant molecule to increase the cytotoxicity of 5‐fluorouracil (5‐FU) through specific inhibition of molecular targets, signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid 2–related factor 2 (Nrf2) in HT‐29 colon cancer...

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Published in:Journal of cellular biochemistry 2019-08, Vol.120 (8), p.14035-14043
Main Authors: Tajmohammadi, Issa, Mohammadian, Jamal, Sabzichi, Mehdi, Mahmuodi, Shiva, Ramezani, Mina, Aghajani, Marjan, Ramezani, Fatemeh
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container_end_page 14043
container_issue 8
container_start_page 14035
container_title Journal of cellular biochemistry
container_volume 120
creator Tajmohammadi, Issa
Mohammadian, Jamal
Sabzichi, Mehdi
Mahmuodi, Shiva
Ramezani, Mina
Aghajani, Marjan
Ramezani, Fatemeh
description We investigated the role of stattic as an adjuvant molecule to increase the cytotoxicity of 5‐fluorouracil (5‐FU) through specific inhibition of molecular targets, signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid 2–related factor 2 (Nrf2) in HT‐29 colon cancer cells. Cytotoxicity and apoptotic effects were investigated by methylthiazolyldiphenyl‐​tetrazolium bromide assay and flow cytometry analysis, respectively. Real‐time polymerase chain reaction was applied to assess the messenger RNA (mRNA) level of STAT3, Nrf2, and apoptotic genes including Bax, Bcl‐xl, and Bcl‐2. The antitumor effect of 5‐FU in combination with stattic induced synergistic effect in HT‐29 cells with combination indexes (CIs) 0.49. Flow cytometric results related to apoptotic confirmed that there was up to 40% increase in the population of apoptotic cells in HT‐29 colon cancer cells incubated with 5‐FU and stattic compared with control groups. Our data from gene expression determined a substantial diminish in the mRNA levels of the Nrf2 and antiapoptotic gene Bcl‐2 along with a noticeable increase in the level of the proapoptotic Bax in HT‐29 colon cells that underwent cotreatment with 5‐FU and stattic (P < 0.05). Moreover, the results exhibited that stattic can be used as adjuvant chemotherapy besides the 5‐FU. This therapeutic approach in colon cancer could mediate 5‐FU chemoresistance via modulating therapeutic targets (ie, STAT3 and Nrf2 pathways) and decreased 5‐FU‐related adverse effects. Stattic boosts the 5‐fluorouracil behavior in human colon cancer
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Cytotoxicity and apoptotic effects were investigated by methylthiazolyldiphenyl‐​tetrazolium bromide assay and flow cytometry analysis, respectively. Real‐time polymerase chain reaction was applied to assess the messenger RNA (mRNA) level of STAT3, Nrf2, and apoptotic genes including Bax, Bcl‐xl, and Bcl‐2. The antitumor effect of 5‐FU in combination with stattic induced synergistic effect in HT‐29 cells with combination indexes (CIs) 0.49. Flow cytometric results related to apoptotic confirmed that there was up to 40% increase in the population of apoptotic cells in HT‐29 colon cancer cells incubated with 5‐FU and stattic compared with control groups. Our data from gene expression determined a substantial diminish in the mRNA levels of the Nrf2 and antiapoptotic gene Bcl‐2 along with a noticeable increase in the level of the proapoptotic Bax in HT‐29 colon cells that underwent cotreatment with 5‐FU and stattic (P &lt; 0.05). Moreover, the results exhibited that stattic can be used as adjuvant chemotherapy besides the 5‐FU. This therapeutic approach in colon cancer could mediate 5‐FU chemoresistance via modulating therapeutic targets (ie, STAT3 and Nrf2 pathways) and decreased 5‐FU‐related adverse effects. 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Cytotoxicity and apoptotic effects were investigated by methylthiazolyldiphenyl‐​tetrazolium bromide assay and flow cytometry analysis, respectively. Real‐time polymerase chain reaction was applied to assess the messenger RNA (mRNA) level of STAT3, Nrf2, and apoptotic genes including Bax, Bcl‐xl, and Bcl‐2. The antitumor effect of 5‐FU in combination with stattic induced synergistic effect in HT‐29 cells with combination indexes (CIs) 0.49. Flow cytometric results related to apoptotic confirmed that there was up to 40% increase in the population of apoptotic cells in HT‐29 colon cancer cells incubated with 5‐FU and stattic compared with control groups. Our data from gene expression determined a substantial diminish in the mRNA levels of the Nrf2 and antiapoptotic gene Bcl‐2 along with a noticeable increase in the level of the proapoptotic Bax in HT‐29 colon cells that underwent cotreatment with 5‐FU and stattic (P &lt; 0.05). Moreover, the results exhibited that stattic can be used as adjuvant chemotherapy besides the 5‐FU. This therapeutic approach in colon cancer could mediate 5‐FU chemoresistance via modulating therapeutic targets (ie, STAT3 and Nrf2 pathways) and decreased 5‐FU‐related adverse effects. 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ispartof Journal of cellular biochemistry, 2019-08, Vol.120 (8), p.14035-14043
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subjects 5‐fluorouracil
apoptosis
Apoptosis - drug effects
bcl-2-Associated X Protein - metabolism
bcl-X Protein - metabolism
Cell Proliferation - drug effects
Cell Survival - drug effects
colon cancer
Colonic Neoplasms - metabolism
Colonic Neoplasms - pathology
combination chemotherapy
combination index
Cyclic S-Oxides - pharmacology
Drug Synergism
Fluorouracil - pharmacology
G1 Phase Cell Cycle Checkpoints - drug effects
Gene Expression Regulation, Neoplastic - drug effects
HT29 Cells
Humans
Inhibitory Concentration 50
NF-E2-Related Factor 2 - metabolism
nuclear factor erythroid 2–related factor 2
RNA, Messenger - genetics
RNA, Messenger - metabolism
signal transducer and activator of transcription 3
STAT3 Transcription Factor - metabolism
stattic
title Identification of Nrf2/STAT3 axis in induction of apoptosis through sub‐G 1 cell cycle arrest mechanism in HT‐29 colon cancer cells
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