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转移相关蛋白磷酸酶-3(PRL-3)的上调引发斑马鱼脊索瘤。

Upregulation of metastasis-associated PRL-3 initiates chordoma in zebrafish.

作者信息

Li Li, Shi Hongshun, Zhang Mingming, Guo Xiaoling, Tong Fang, Zhang Wenliang, Zhou Junyi, Wang Haihe, Yang Shulan

机构信息

Translational Medicine Centre, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong CPZN 510080, P.R. China.

Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong CPZN 510080, P.R. China.

出版信息

Int J Oncol. 2016 Apr;48(4):1541-52. doi: 10.3892/ijo.2016.3363. Epub 2016 Jan 29.

Abstract

The metastasis-associated phosphatase of regenerating liver-3 (PRL-3) plays multiple roles in progression of various human cancers; however, significance of its role during development has not been addressed. Here we cloned and characterized the expression pattern of zebrafish prl-3 transcript and showed that it is ubiquitiously expressed in the first 24 h of development with both maternal and zygotic expressions. The transcripts become progressively restricted to the notochord, vessels and the intestine by 96 h post-fertilization. Notably, overexpression of zebrafish Prl-3 (zPrl-3) and human PRL-3 induces notochord malformation in zebrafish. This phenotype resembles chordoma and is confirmed by associated misexpression of notochord-specific markers. Clinical significance of the PRL-3 in chordoma is strongly suggested by detection of PRL-3 antigen in clinical chordoma specimens. Collectively, our results uncovered that aberrant overexpression of PRL-3 could initiate chordoma in early development and suggest the use of PRL-3 could be used as a predictor and a therapeutic target for chordoma.

摘要

再生肝脏-3转移相关磷酸酶(PRL-3)在多种人类癌症进展中发挥多种作用;然而,其在发育过程中的作用意义尚未得到探讨。在此,我们克隆并表征了斑马鱼prl-3转录本的表达模式,结果显示它在发育的最初24小时内通过母源和合子表达而广泛表达。受精后96小时,转录本逐渐局限于脊索、血管和肠道。值得注意的是,斑马鱼Prl-3(zPrl-3)和人类PRL-3的过表达会诱导斑马鱼脊索畸形。这种表型类似于脊索瘤,并通过脊索特异性标记物的相关错误表达得到证实。临床脊索瘤标本中PRL-3抗原的检测强烈提示了PRL-3在脊索瘤中的临床意义。总体而言,我们的结果揭示PRL-3的异常过表达可在早期发育中引发脊索瘤,并提示PRL-3可作为脊索瘤的预测指标和治疗靶点。

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