Perez-Pinera Pablo, Chang Yunchao, Deuel Thomas F
The Scripps Research Institute, La Jolla, California 92037, USA.
Cell Cycle. 2007 Dec 1;6(23):2877-83. doi: 10.4161/cc.6.23.5090.
Pleiotrophin (PTN, Ptn) is a widely expressed, developmentally regulated 136 amino acid secreted heparin-binding cytokine. It signals through a unique signaling pathway; the PTN receptor is the transmembrane receptor protein tyrosine phosphatase (RPTP)beta/zeta. RPTPbeta/zeta is inactivated by PTN, which leads to increased tyrosine phosphorylation of the downstream targets of the PTN/RPTPbeta/zeta signaling pathway. Pleiotrophin gene expression is found in cells in early differentiation during different developmental periods. It is upregulated in cells with an early differentiation phenotype in wound repair. The Ptn gene also is a proto-oncogene; PTN is expressed in human tumor cells, and, in cell lines derived from human tumors that express Ptn, Ptn expression is constitutive and thus "inappropriate". Importantly, properties of different cells induced by PTN in PTN-stimulated cells are strikingly similar to properties of highly malignant cells. Furthermore, transformed cells into which Ptn is introduced undergo "switches" to malignant cells of higher malignancy with properties that are strikingly similar to properties of PTN-stimulated cells. These unique features of PTN support the conclusion that constitutive PTN signaling in malignant cells that inappropriately express Ptn functions as a potent tumor promoter. Recently, in confirmation, Ptn targeted by the mouse mammary tumor virus (MMTV) promoter in a transgenic mouse model was found to promote breast cancers to a more aggressive breast cancer cell phenotype that morphologically closely resembles scirrhous carcinoma in human; in addition, it promoted a striking increase in tumor angiogenesis and a remarkable degree of remodeling of the micro-environment. Pleiotrophin thus regulates both different normal and pathological functions; collectively, the different studies have uncovered the unique ability of a single cytokine PTN, which signals through the unique PTN/RPTPbeta/zeta signaling pathway, to induce the many properties associated with tumor promotion in the malignant cells that constitutively express Ptn and in their microenvironment.
多效生长因子(PTN,Ptn)是一种广泛表达、受发育调控的含136个氨基酸的分泌型肝素结合细胞因子。它通过一条独特的信号通路进行信号传导;PTN受体是跨膜受体蛋白酪氨酸磷酸酶(RPTP)β/ζ。PTN可使RPTPβ/ζ失活,这会导致PTN/RPTPβ/ζ信号通路下游靶点的酪氨酸磷酸化增加。在不同发育阶段的早期分化细胞中可发现多效生长因子基因表达。在伤口修复过程中,具有早期分化表型的细胞中该基因表达上调。Ptn基因也是一种原癌基因;PTN在人类肿瘤细胞中表达,并且在源自表达Ptn的人类肿瘤的细胞系中,Ptn的表达是组成性的,因此是“不适当的”。重要的是,PTN在PTN刺激的细胞中诱导的不同细胞特性与高恶性细胞的特性惊人地相似。此外,导入Ptn的转化细胞会“转变”为恶性程度更高的恶性细胞,其特性与PTN刺激的细胞的特性惊人地相似。PTN的这些独特特征支持这样的结论:在不适当表达Ptn的恶性细胞中,组成性的PTN信号传导起到了强大的肿瘤促进作用。最近,在转基因小鼠模型中,由小鼠乳腺肿瘤病毒(MMTV)启动子靶向的Ptn被发现可促使乳腺癌转变为更具侵袭性的乳腺癌细胞表型,其形态与人类硬癌非常相似;此外,它还促使肿瘤血管生成显著增加以及微环境发生显著重塑。因此,多效生长因子调节不同的正常和病理功能;总体而言,不同的研究揭示了单一细胞因子PTN通过独特的PTN/RPTPβ/ζ信号通路进行信号传导,从而在组成性表达Ptn的恶性细胞及其微环境中诱导许多与肿瘤促进相关特性的独特能力。