TY - JOUR
T1 - Allyl isothiocyanate exhibits no anticancer activity in MDA-MB-231 breast cancer cells
AU - Sayeed, Md Abu
AU - Bracci, Massimo
AU - Ciarapica, Veronica
AU - Malavolta, Marco
AU - Provinciali, Mauro
AU - Pieragostini, Ernesta
AU - Gaetani, Simona
AU - Monaco, Federica
AU - Lucarini, Guendalina
AU - Rapisarda, Venerando
AU - Di Primio, Roberto
AU - Santarelli, Lory
PY - 2018/1/4
Y1 - 2018/1/4
N2 - It was reported recently that allyl isothiocyanate (AITC) could inhibit various types of cancer cell growth. In the present study, we further investigated whether AITC could inhibit the growth of human breast cancer cells. Unexpectedly, we found that AITC did not inhibit, rather slightly promoted, the proliferation of MDA-MB-231 breast cancer cells, although it did have inhibitory effect on MCF-7 breast cancer cells. Cytofluorimetric analysis revealed that AITC (10 µM) did not induce apoptosis and cell cycle arrest in MDA-MB-231 cells. In addition, AITC significantly (p < 0.05) increased the expression of BCL-2 and mTOR genes and Beclin-1 protein in MDA-MB-231 cells. No significant changes in expression of PRKAA1 and PER2 genes, Caspase-8, Caspase-9, PARP, p-mTOR, and NF-κB p65 proteins were observed in these AITC-treated cells. Importantly, AITC displayed cytotoxic effect on MCF-10A human breast epithelial cell line. These observations suggest that AITC may not have inhibitory activity in MDA-MB-231 breast cancer cells. This in vitro study warrants more preclinical and clinical studies on the beneficial and harmful effects of AITC in healthy and cancer cells.
AB - It was reported recently that allyl isothiocyanate (AITC) could inhibit various types of cancer cell growth. In the present study, we further investigated whether AITC could inhibit the growth of human breast cancer cells. Unexpectedly, we found that AITC did not inhibit, rather slightly promoted, the proliferation of MDA-MB-231 breast cancer cells, although it did have inhibitory effect on MCF-7 breast cancer cells. Cytofluorimetric analysis revealed that AITC (10 µM) did not induce apoptosis and cell cycle arrest in MDA-MB-231 cells. In addition, AITC significantly (p < 0.05) increased the expression of BCL-2 and mTOR genes and Beclin-1 protein in MDA-MB-231 cells. No significant changes in expression of PRKAA1 and PER2 genes, Caspase-8, Caspase-9, PARP, p-mTOR, and NF-κB p65 proteins were observed in these AITC-treated cells. Importantly, AITC displayed cytotoxic effect on MCF-10A human breast epithelial cell line. These observations suggest that AITC may not have inhibitory activity in MDA-MB-231 breast cancer cells. This in vitro study warrants more preclinical and clinical studies on the beneficial and harmful effects of AITC in healthy and cancer cells.
KW - Allyl isothiocyanate
KW - Apoptosis
KW - Breast cancer
KW - Cell cycle
KW - Proliferation
UR - http://www.scopus.com/inward/record.url?scp=85041819842&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85041819842&partnerID=8YFLogxK
U2 - 10.3390/ijms19010145
DO - 10.3390/ijms19010145
M3 - Article
C2 - 29300316
AN - SCOPUS:85041819842
SN - 1661-6596
VL - 19
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 1
M1 - 145
ER -