TY - JOUR
T1 - Cancer cell death induced by the intracellular self-assembly of an enzyme-responsive supramolecular gelator
AU - Tanaka, Akiko
AU - Fukuoka, Yuki
AU - Morimoto, Yuka
AU - Honjo, Takafumi
AU - Koda, Daisuke
AU - Goto, Masahiro
AU - Maruyama, Tatsuo
N1 - Publisher Copyright:
© 2014 American Chemical Society.
PY - 2015/1/21
Y1 - 2015/1/21
N2 - We report cancer cell death initiated by the intracellular molecular self-assembly of a peptide lipid, which was derived from a gelator precursor. The gelator precursor was designed to form nanofibers via molecular self-assembly, after cleavage by a cancer-related enzyme (matrix metalloproteinase-7, MMP-7), leading to hydrogelation. The gelator precursor exhibited remarkable cytotoxicity to five different cancer cell lines, while the precursor exhibited low cytotoxicity to normal cells. Cancer cells secrete excessive amounts of MMP-7, which converted the precursor into a supramolecular gelator prior to its uptake by the cells. Once inside the cells, the supramolecular gelator formed a gel via molecular self-assembly, exerting vital stress on the cancer cells. The present study thus describes a new drug where molecular self-assembly acts as the mechanism of cytotoxicity.
AB - We report cancer cell death initiated by the intracellular molecular self-assembly of a peptide lipid, which was derived from a gelator precursor. The gelator precursor was designed to form nanofibers via molecular self-assembly, after cleavage by a cancer-related enzyme (matrix metalloproteinase-7, MMP-7), leading to hydrogelation. The gelator precursor exhibited remarkable cytotoxicity to five different cancer cell lines, while the precursor exhibited low cytotoxicity to normal cells. Cancer cells secrete excessive amounts of MMP-7, which converted the precursor into a supramolecular gelator prior to its uptake by the cells. Once inside the cells, the supramolecular gelator formed a gel via molecular self-assembly, exerting vital stress on the cancer cells. The present study thus describes a new drug where molecular self-assembly acts as the mechanism of cytotoxicity.
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U2 - 10.1021/ja510156v
DO - 10.1021/ja510156v
M3 - Article
C2 - 25521540
AN - SCOPUS:84921511395
SN - 0002-7863
VL - 137
SP - 770
EP - 775
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 2
ER -