Broccoli extract improves chemotherapeutic drug efficacy against head-neck squamous cell carcinomas

被引:19
作者
Elkashty, Osama A. [1 ,2 ]
Ashry, Ramy [2 ]
Abu Eighanam, Ghada [1 ,3 ]
Pham, Hieu M. [1 ]
Su, Xinyun [1 ,4 ]
Stegen, Camille [5 ,6 ]
Tran, Simon D. [1 ]
机构
[1] McGill Univ, Fac Dent, McGill Craniofacial Tissue Engn & Stem Cells Lab, 3640 Univ St, Montreal, PQ H3A 0C7, Canada
[2] Mansoura Univ, Fac Dent, Oral Pathol Dept, Mansoura, Egypt
[3] Univ Jordan, Fac Med, Amman, Jordan
[4] Guangxi Med Univ, Coll Stomatol, Nanning, Guangxi, Peoples R China
[5] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[6] McGill Univ, Microbiome & Dis Tolerance Ctr, Montreal, PQ, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
Head and Neck cancer; Carcinoma; squamous cell; Sulforaphane; Drug therapy; Apoptosis; DNA damage; CANCER STATISTICS; SULFORAPHANE; CISPLATIN; MECHANISMS; APOPTOSIS; ISOTHIOCYANATE; SENSITIVITY; RESISTANCE; PROTEIN; LEADS;
D O I
10.1007/s12032-018-1186-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The efficacy of cisplatin (CIS) and 5-fluorouracil (5-FU) against squamous cell carcinomas of the head and neck (SCCHN) remains restricted due to their severe toxic side effects on non-cancer (normal) tissues. Recently, the broccoli extract sulforaphane (SF) was successfully tested as a combination therapy to target cancer cells. However, the effect of lower doses of CIS or 5-FU combined with SF on SCCHN remained unknown. This study tested the chemotherapeutic efficacies of SF combined with much lower doses of CIS or 5-FU against SCCHN cells aiming to reduce cytotoxicity to normal cells. Titrations of SF standalone or in combination with CIS and 5-FU were tested on SCCHN human cell lines (SCC12 and SCC38) and non-cancerous human cells (fibroblasts, gingival, and salivary cells). Concentrations of SF tested were comparable to those found in the plasma following ingestion of fresh broccoli sprouts. The treatment effects on cell viability, proliferation, DNA damage, apoptosis, and gene expression were measured. SF reduced SCCHN cell viability in a time- and dose-dependent manner. SF-combined treatment increased the cytotoxic activity of CIS by twofolds and of 5-FU by tenfolds against SCCHN, with no effect on non-cancerous cells. SF-combined treatment inhibited SCCHN cell clonogenicity and post-treatment DNA repair. SF increased SCCHN apoptosis and this mechanism was due to a down-regulation of BCL2 and up-regulation of BAX, leading to an up-regulation of Caspase3. In conclusion, combining SF with low doses of CIS or 5-FU increased cytotoxicity against SCCHN cells, while having minimal effects on normal cells.
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页数:10
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