Shigeo Takaishi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Shigeo Takaishi has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
Aiko Sugiyama
DSK Project, Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan
1 shared publicationAkihiko Yoshizawa
Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan
1 shared publicationAkitada Yogo
DSK Project, Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan
1 shared publicationHiroshi Seno
DSK Project, Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan
1 shared publicationKenji Masuo
DSK Project, Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan
1 shared publication- Ru Chen
DSK Project, Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan
1 shared publication
Latest Publications
- 12 December 2020
- Published by Oxford University Press (OUP) in Carcinogenesis
- Vol. 42 (2) , 190-201
SNAIL regulates gastric carcinogenesis through CCN3 and NEFL
Among cancer cells, there are specific cell populations of whose activities are comparable to those of stem cells in normal tissues, and for whom the levels of cell dedifferentiation are reported to correlate with poor prognosis. Information concerning the mechanisms that modulate the stemness like traits of cancer cells is limited. Therefore, we examined five gastric cancer cell lines and isolated gastric oncospheres from three gastric cancer cell lines. The gastric cancer cells that expanded in the spheres expressed relatively elevated proportion of CD44, which is a marker of gastric cancer stem cells (CSCs), and displayed many properties of CSCs, for example: chemoresistance, tumorigenicity and epithelial–mesenchymal transition (EMT) acquisition. SNAIL, which is a key factor in EMT, was highly expressed in the gastric spheres. Microarray analysis in gastric cancer cell line HGC27 showed that CCN3 and NEFL displayed the greatest differential expression by knocking down of SNAIL; the former was upregulated and the latter downregulated, respectively. Downregulation of CCN3 and upregulation of NEFL gene expression impaired the SNAIL-dependent EMT activity: high tumorigenicity, and chemoresistance in gastric cancer cells. Thus, approach that disrupts SNAIL/CCN3/NEFL axis may be credible in inhibiting gastric cancer development.
- 12 December 2020
- Published by Oxford University Press (OUP) in Carcinogenesis
- Vol. 42 (2) , 190-201
SNAIL regulates gastric carcinogenesis through CCN3 and NEFL
Among cancer cells, there are specific cell populations of whose activities are comparable to those of stem cells in normal tissues, and for whom the levels of cell dedifferentiation are reported to correlate with poor prognosis. Information concerning the mechanisms that modulate the stemness like traits of cancer cells is limited. Therefore, we examined five gastric cancer cell lines and isolated gastric oncospheres from three gastric cancer cell lines. The gastric cancer cells that expanded in the spheres expressed relatively elevated proportion of CD44, which is a marker of gastric cancer stem cells (CSCs), and displayed many properties of CSCs, for example: chemoresistance, tumorigenicity and epithelial–mesenchymal transition (EMT) acquisition. SNAIL, which is a key factor in EMT, was highly expressed in the gastric spheres. Microarray analysis in gastric cancer cell line HGC27 showed that CCN3 and NEFL displayed the greatest differential expression by knocking down of SNAIL; the former was upregulated and the latter downregulated, respectively. Downregulation of CCN3 and upregulation of NEFL gene expression impaired the SNAIL-dependent EMT activity: high tumorigenicity, and chemoresistance in gastric cancer cells. Thus, approach that disrupts SNAIL/CCN3/NEFL axis may be credible in inhibiting gastric cancer development.