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Differential Pharmacological Activities of Oxygen Numbers on the Sulfoxide Moiety of Wasabi Compound 6-(Methylsulfinyl) Hexyl Isothiocyanate in Human Oral Cancer Cells.
Lee, Min-Ju; Tseng, Wen-Ser; Lai, Jerry Cheng-Yen; Shieh, Hui-Ru; Chi, Chih-Wen; Chen, Yu-Jen.
Affiliation
  • Lee MJ; Taipei First Girls High School, Taipei 10045, Taiwan. minrulee0908@gmail.com.
  • Tseng WS; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan. selene0508@hotmail.com.
  • Lai JC; Department of Medical Research, Taitung MacKay Memorial Hospital, Taitung City 95054, Taiwan. chengyen@hotmail.com.
  • Shieh HR; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan. ru123@mmh.org.tw.
  • Chi CW; Department of Medical Research, MacKay Memorial Hospital, New Taipei City 25160, Taiwan. cwchid48906003@gmail.com.
  • Chen YJ; Department of Nursing, MacKay Medical College, New Taipei City 25245, Taiwan. cwchid48906003@gmail.com.
Molecules ; 23(10)2018 Sep 21.
Article in En | MEDLINE | ID: mdl-30248933
6-(methylsulfinyl) hexyl isothiocyanate (6-MITC) is a naturally occurring compound isolated from Wasabia japonica (wasabi). The synthetic derivatives, 6-(methylsulfenyl) hexyl isothiocyanate (I7447) and 6-(methylsulfonyl) hexyl isothiocyanate (I7557), were derived from 6-MITC with the deletion and addition of oxygen, respectively. We aimed to evaluate the effect of these synthetic compounds on human oral cancer cells, SAS and OECM-1. All three compounds (I7447, 6-MITC, and I7557) inhibited the viability of SAS and OECM-1 cells using MTT assay. Morphological observations showed various proportions of mitotic arrest and apoptosis in cells treated with these compounds. Cell cycle analysis revealed relatively abundant G2/M arrest in 6-MITC and I7557-treated cells, whereas sub-G1 accumulation was found in I7447-treated cells. In using phosphorylated histone H3 as a marker for mitosis, the addition of 6-MITC and I7557 (excluding I7447) could be shown to arrest cells during mitosis. In contrast, I7447 induced more prominent apoptosis than the 6-MITC or I7557 compounds. The down-regulated expression of the phosphorylated form of CHK1 and Cdc25c was noted in 6-MITC and I7557-treated cells. I7557 could sensitize SAS cells to death by radiation. The wasabi compound, 6-MITC, and its chemical derivatives with different numbers of oxygen may have differential pharmacological effects on human oral cancer cells.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mouth Neoplasms / Isothiocyanates / Cdc25 Phosphatases / Wasabia / Checkpoint Kinase 1 / Antineoplastic Agents Limits: Humans Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2018 Document type: Article Affiliation country: Taiwan Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mouth Neoplasms / Isothiocyanates / Cdc25 Phosphatases / Wasabia / Checkpoint Kinase 1 / Antineoplastic Agents Limits: Humans Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2018 Document type: Article Affiliation country: Taiwan Country of publication: Switzerland