Establishment of an oral squamous cell carcinoma cell line expressing vascular endothelial growth factor a and its two receptors.
Establishment of an oral squamous cell carcinoma cell line expressing vascular endothelial growth factor a and its two receptors.
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表达血管内皮生长因子a及其两种受体的口腔鳞状细胞癌细胞系的建立。
DOI:
10.1016/j.jds.2022.04.018
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发表时间:
2022-10
影响因子:
3.5
通讯作者:
Kishimoto, Hiromitsu
中科院分区:
文献类型:
--
作者:
Araki-Maeda, Hanako;Kawabe, Mutsuki;Omori, Yuji;Yamanegi, Koji;Yoshida, Kazunari;Yoshikawa, Kyohei;Takaoka, Kazuki;Noguchi, Kazuma;Nakano, Yoshiro;Kishimoto, Hiromitsu
Vascular endothelial growth factor receptor (VEGFR) expression in oral squamous cell carcinoma (OSCC) promotes tumor growth through both autocrine and paracrine signaling. VEGF-positive OSCC cases are associated with a high depth of invasion, increased metastasis, and poor prognosis. In this study we established and then molecularly and functionally analyzed an OSCC cell line that co-expresses VEGF-A, VEGFR-1, and VEGFR-2, termed HCM-SqCC010 cells. VEGF-A, VEGFR-1, and VEGFR-2 expression in HCM-SqCC010 cells were examined by immunohistochemistry and immunoblotting. Expression and inhibition of VEGF-A, VEGFR-1, and VEGFR-2 in HCM-SqCC010 cells were verified by quantitative real-time PCR. Our analysis of HCM-SqCC010 cells revealed that their proliferation depended on VEGF-A, and selective inhibition of VEGFR-1 or VEGFR-2 resulted in decreased cell growth. We established an OSCC cell line, HCM-SqCC010, that expresses VEGF-A, VEGFR-1, and VEGFR-2. This triple-positive cell line showed no effect from a molecular targeted drug toward VEGF-A, but it did show strong cell growth inhibition in response to a VEGFR inhibitor. Thus, new therapeutic strategies against OSCC should include a VEGFR inhibitor.
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影响因子:
4.3
作者:
Knizetova, Petra;Ehrmann, Jiri;Bartek, Jiri
通讯作者:
Bartek, Jiri
影响因子:
3.6
作者:
Mohamed, KM;Le, A;Messadi, DV
通讯作者:
Messadi, DV
影响因子:
21.3
作者:
Costa-Silva B;Aiello NM;Ocean AJ;Singh S;Zhang H;Thakur BK;Becker A;Hoshino A;Mark MT;Molina H;Xiang J;Zhang T;Theilen TM;García-Santos G;Williams C;Ararso Y;Huang Y;Rodrigues G;Shen TL;Labori KJ;Lothe IM;Kure EH;Hernandez J;Doussot A;Ebbesen SH;Grandgenett PM;Hollingsworth MA;Jain M;Mallya K;Batra SK;Jarnagin WR;Schwartz RE;Matei I;Peinado H;Stanger BZ;Bromberg J;Lyden D
通讯作者:
Lyden D
影响因子:
64.5
作者:
Lichtenberger, Beate M.;Tan, Poi Kiang;Sibilia, Maria
通讯作者:
Sibilia, Maria
影响因子:
1.2
作者:
Noguchi K;Kanda S;Yoshida K;Funaoka Y;Yamanegi K;Yoshikawa K;Takaoka K;Kishimoto H;Nakano Y
通讯作者:
Nakano Y