Premium
Melatonin increases the anticancer potential of doxorubicin in Caco‐2 colorectal cancer cells
Author(s) -
Jadid Mahdieh Farhoudi Sefidan,
Aghaei Elnaz,
Taheri Elham,
Seyyedsani Nasrin,
Chavoshi Reza,
Abbasi Samane,
Khorrami Afshin,
Goleij Pouya,
Hajazimian Saba,
Taefehshokr Sina,
Isazadeh Alireza,
Shanehbandi Dariush
Publication year - 2021
Publication title -
environmental toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.813
H-Index - 77
eISSN - 1522-7278
pISSN - 1520-4081
DOI - 10.1002/tox.23105
Subject(s) - melatonin , doxorubicin , apoptosis , survivin , viability assay , colorectal cancer , cancer research , pharmacology , flow cytometry , cancer cell , biology , cancer , chemistry , medicine , chemotherapy , immunology , biochemistry
Colorectal cancer (CC) is an important human malignancy with high cancer related death worldwide. The chemotherapy using doxorubicin hydrochloride is one of the most common cancer therapeutic methods. However, drug resistance lowers the treatment efficacy in CC patients. The combination therapies seem to be more promising by taking the advantage of synergistic effects. The present study aimed to evaluate a new strategy to enhance the anticancer activity of doxorubicin in Caco‐2 CC cell line by co‐administration of melatonin. The effects of doxorubicin, melatonin, and their combinations (Dox‐Mel) were investigated on the proliferation and viability, morphological alterations, and tumor spheroid formation. Flow cytometry was employed to compare the apoptotic situation of the cells in study groups. Changes in metastatic potential of the cells were assessed by wound healing assay and trans‐well migration assays. Moreover, expression of BAX , SMAC , BCL‐2 , SURVIVIN , MMP‐2 , and MMP‐9 genes were evaluated by quantitative real time PCR and western blotting. Our study showed that doxorubicin, melatonin, and Dox‐Mel significantly decreased the proliferation and viability, tumor spheroid formation, invasion, and migration. Furthermore, the changes were in a concentration and time dependent manner. There was an increase in apoptosis rate in the treatment groups. Expression of genes involved in apoptosis and cell motility were altered significantly. It was observed that anticancer activity of Dox‐Mel combination was significantly more than doxorubicin and melatonin treatments alone. We showed an enhanced apoptotic and anticancer activity of doxorubicin and melatonin combination chemotherapy on CC cell line than doxorubicin or melatonin treatments alone. This combination could promote the treatment efficiency and alleviate the un‐intended side effects by lowering the dose of doxorubicin prescription.