TY - JOUR
T1 - Effect of the orthoquinone moiety in 9,10-phenanthrenequinone on its ability to induce apoptosis in HCT-116 and HL-60 cells
AU - Hatae, Noriyuki
AU - Nakamura, Jun
AU - Okujima, Tetsuo
AU - Ishikura, Minoru
AU - Abe, Takumi
AU - Hibino, Satoshi
AU - Choshi, Tominari
AU - Okada, Chiaki
AU - Yamada, Hiroko
AU - Uno, Hidemitsu
AU - Toyota, Eiko
N1 - Funding Information:
This study was partly supported by a Grant-in Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture of Japan .
PY - 2013/8/15
Y1 - 2013/8/15
N2 - 9,10-Phenanthrenequinone (9,10-PQ) is one of the most abundant quinones among diesel exhaust particulates. Recent data have suggested that quinones induce apoptosis in immune, epithelial and tumor cells, leading to respirator illness; however, the mechanisms by which quinones induce apoptosis and the structure required for this remain unknown. We studied the antitumor activity of 9,10-PQ analogs against two human tumor cell lines, HCT-116 colon tumor cells and HL-60 promyelocytic leukemia cells. The loss of the cis-orthoquinone unit in 9,10-PQ abrogated its ability to induce apoptosis in the two tumor cell lines, and the LC50 values of these analogs were indicated over 10 μM. An analog of 9,10-PQ in which the biaryl unit had been deleted displayed a reduced ability to induce tumor cell apoptosis, while the analogs 1,10-phenanthroline- 5,6-dione (9) and pyrene-4,5-dione (10), which also had modified biaryl units, exhibited increased tumor cell apoptotic activity. The cis-orthoquinone unit in 9,10-PQ was identified as essential for its ability to induce apoptosis in tumor cells, and its biaryl unit is also considered to influence orthoquinone- mediated apoptotic activity.
AB - 9,10-Phenanthrenequinone (9,10-PQ) is one of the most abundant quinones among diesel exhaust particulates. Recent data have suggested that quinones induce apoptosis in immune, epithelial and tumor cells, leading to respirator illness; however, the mechanisms by which quinones induce apoptosis and the structure required for this remain unknown. We studied the antitumor activity of 9,10-PQ analogs against two human tumor cell lines, HCT-116 colon tumor cells and HL-60 promyelocytic leukemia cells. The loss of the cis-orthoquinone unit in 9,10-PQ abrogated its ability to induce apoptosis in the two tumor cell lines, and the LC50 values of these analogs were indicated over 10 μM. An analog of 9,10-PQ in which the biaryl unit had been deleted displayed a reduced ability to induce tumor cell apoptosis, while the analogs 1,10-phenanthroline- 5,6-dione (9) and pyrene-4,5-dione (10), which also had modified biaryl units, exhibited increased tumor cell apoptotic activity. The cis-orthoquinone unit in 9,10-PQ was identified as essential for its ability to induce apoptosis in tumor cells, and its biaryl unit is also considered to influence orthoquinone- mediated apoptotic activity.
KW - 9,10-Phenanthrenequinone
KW - Antitumor activity
KW - Apoptosis
KW - Diesel exhaust particulates
KW - Orthoquinone
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U2 - 10.1016/j.bmcl.2013.06.015
DO - 10.1016/j.bmcl.2013.06.015
M3 - Article
C2 - 23816373
AN - SCOPUS:84880604414
SN - 0960-894X
VL - 23
SP - 4637
EP - 4640
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
IS - 16
ER -