TY - JOUR
T1 - Novel drug discovery system for cancer stem cells in human squamous cell carcinoma of the esophagus
AU - Kano, Yoshihiro
AU - Konno, Masamitsu
AU - Kawamoto, Koichi
AU - Tamari, Keisuke
AU - Hayashi, Kazuhiko
AU - Fukusumi, Takahito
AU - Satoh, Taroh
AU - Tanaka, Shinji
AU - Ogawa, Kazuhiko
AU - Mori, Masaki
AU - Doki, Yuichiro
AU - Ishii, Hideshi
PY - 2014/3
Y1 - 2014/3
N2 - Cancer stem cells (CSCs) have been identified in several tumor tissues. Since CSCs are resistant to cancer therapies, including chemotherapy and radiation therapy, and can even remain after therapies, tumor tissue often regrows and relapses. Thus, identification of CSCs and treatment targeting CSCs are required to treat tumor tissues. Reportedly, a fluorescent vector consisting of fluorescein ZsGreen fused to the carboxyl-terminal region of ornithine decarboxylase (cODC) was used to detect CSCs or therapy-resistant cancer cells in tumor tissues of the brain, pancreas and liver. Cells transfected with the fluorescent vector can express a fluorescein fused to cODC and become fluorescent only when the fusion protein is accumulated. In the present study, CSCs or therapy-resistant cancer cells were identified with the fluorescent vector in esophageal squamous cell carcinoma. The use of this fluorescent vector in drug screening enabled the detection of three drugs, AKT inhibitor XI, ERK inhibitor II and JAK inhibitor I, which target malignant CSCs.
AB - Cancer stem cells (CSCs) have been identified in several tumor tissues. Since CSCs are resistant to cancer therapies, including chemotherapy and radiation therapy, and can even remain after therapies, tumor tissue often regrows and relapses. Thus, identification of CSCs and treatment targeting CSCs are required to treat tumor tissues. Reportedly, a fluorescent vector consisting of fluorescein ZsGreen fused to the carboxyl-terminal region of ornithine decarboxylase (cODC) was used to detect CSCs or therapy-resistant cancer cells in tumor tissues of the brain, pancreas and liver. Cells transfected with the fluorescent vector can express a fluorescein fused to cODC and become fluorescent only when the fusion protein is accumulated. In the present study, CSCs or therapy-resistant cancer cells were identified with the fluorescent vector in esophageal squamous cell carcinoma. The use of this fluorescent vector in drug screening enabled the detection of three drugs, AKT inhibitor XI, ERK inhibitor II and JAK inhibitor I, which target malignant CSCs.
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U2 - 10.3892/or.2013.2952
DO - 10.3892/or.2013.2952
M3 - Article
C2 - 24378718
AN - SCOPUS:84896694472
SN - 1021-335X
VL - 31
SP - 1133
EP - 1138
JO - Oncology reports
JF - Oncology reports
IS - 3
ER -