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促甲状腺激素通过激活蛋白激酶C而非蛋白激酶A来刺激甲状腺滤泡癌细胞的侵袭和生长。

Thyrotropin stimulates invasion and growth of follicular thyroid cancer cells via PKC- rather than PKA-activation.

作者信息

Hoelting T, Tezelman S, Siperstein A E, Duh Q Y, Clark O H

机构信息

Surgical Service, Veterans Affairs Medical Center, San Francisco, CA.

出版信息

Biochem Biophys Res Commun. 1993 Sep 30;195(3):1230-6. doi: 10.1006/bbrc.1993.2176.

Abstract

The signal transduction of TSH in invasion and growth of FTC 133, a human follicular thyroid cancer cell line, was investigated. TSH (0.01-1 mIU/ml) stimulated invasion of FTC 133 by 21% and growth by 20% of basal. Cyclic AMP-stimulators and inhibitors had no effect at any concentration. The PKC-agonist TPA enhanced invasion and growth by 15%, whereas staurosporine, a PKC-antagonist, inhibited them by 32% and 60%, respectively. The latter also reversed TSH stimulation. EGF enhanced invasion (42%) and growth of FTC 133 (25%). Staurosporine did not reverse EGF stimulation. The tyrosine kinase antagonist genistein reversed EGF, but not TSH stimulation. Pertussis toxin inhibited invasion (18%) and growth (22%). Cholera toxin was less inhibitive. We demonstrated for the first time, that TSH stimulates invasion and growth of human thyroid cancer cells in vitro by PKC- rather than PKA-stimulation.

摘要

研究了促甲状腺激素(TSH)在人甲状腺滤泡癌细胞系FTC 133侵袭和生长中的信号转导。TSH(0.01 - 1 mIU/ml)刺激FTC 133的侵袭增加21%,生长比基础水平增加20%。环磷酸腺苷(cAMP)刺激剂和抑制剂在任何浓度下均无作用。蛋白激酶C(PKC)激动剂佛波酯(TPA)使侵袭和生长分别增强15%,而PKC拮抗剂星形孢菌素分别使其抑制32%和60%。后者还能逆转TSH的刺激作用。表皮生长因子(EGF)增强FTC 133的侵袭(42%)和生长(25%)。星形孢菌素不能逆转EGF的刺激作用。酪氨酸激酶拮抗剂染料木黄酮能逆转EGF的刺激作用,但不能逆转TSH的刺激作用。百日咳毒素抑制侵袭(18%)和生长(22%)。霍乱毒素的抑制作用较小。我们首次证明,TSH在体外通过刺激PKC而非蛋白激酶A(PKA)来刺激人甲状腺癌细胞的侵袭和生长。

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