Laboratory of Cancer Pathology, Center for Advanced Studies and Technology (CAST), University 'G. D'Annunzio', Chieti, Italy; Department of Medical, Oral and Biotechnological Sciences, University 'G. d'Annunzio', Chieti, Italy.
Laboratory of Cancer Pathology, Center for Advanced Studies and Technology (CAST), University 'G. D'Annunzio', Chieti, Italy.
Neoplasia. 2021 Apr;23(4):415-428. doi: 10.1016/j.neo.2021.03.006. Epub 2021 Apr 8.
Trop-2 is a transmembrane signal transducer that can induce cancer growth. Using antibody targeting and N-terminal Edman degradation, we show here that Trop-2 undergoes cleavage in the first thyroglobulin domain loop of its extracellular region, between residues R87 and T88. Molecular modeling indicated that this cleavage induces a profound rearrangement of the Trop-2 structure, which suggested a deep impact on its biological function. No Trop-2 cleavage was detected in normal human tissues, whereas most tumors showed Trop-2 cleavage, including skin, ovary, colon, and breast cancers. Coimmunoprecipitation and mass spectrometry analysis revealed that ADAM10 physically interacts with Trop-2. Immunofluorescence/confocal time-lapse microscopy revealed that the two molecules broadly colocalize at the cell membrane. We show that ADAM10 inhibitors, siRNAs and shRNAs abolish the processing of Trop-2, which indicates that ADAM10 is an effector protease. Proteolysis of Trop-2 at R87-T88 triggered cancer cell growth both in vitro and in vivo. A corresponding role was shown for metastatic spreading of colon cancer, as the R87A-T88A Trop-2 mutant abolished xenotransplant metastatic dissemination. Activatory proteolysis of Trop-2 was recapitulated in primary human breast cancers. Together with the prognostic impact of Trop-2 and ADAM10 on cancers of the skin, ovary, colon, lung, and pancreas, these data indicate a driving role of this activatory cleavage of Trop-2 on malignant progression of tumors.
Trop-2 是一种跨膜信号转导蛋白,可诱导癌症生长。通过抗体靶向和 N 端 Edman 降解,我们在此表明 Trop-2 在其细胞外区域的第一个甲状腺球蛋白结构域环中发生裂解,位于残基 R87 和 T88 之间。分子建模表明这种裂解诱导 Trop-2 结构的深刻重排,这表明对其生物学功能有深远影响。在正常的人类组织中未检测到 Trop-2 裂解,而大多数肿瘤显示出 Trop-2 裂解,包括皮肤、卵巢、结肠和乳腺癌。共免疫沉淀和质谱分析显示 ADAM10 与 Trop-2 物理相互作用。免疫荧光/共聚焦延时显微镜显示这两个分子广泛在细胞膜上共定位。我们表明 ADAM10 抑制剂、siRNA 和 shRNA 可消除 Trop-2 的加工,这表明 ADAM10 是一种效应蛋白酶。Trop-2 在 R87-T88 处的蛋白水解触发了体外和体内的癌细胞生长。结肠癌转移扩散的相应作用表明,R87A-T88A Trop-2 突变体消除了异种移植转移的扩散。Trop-2 的激活性蛋白水解在原发性人乳腺癌中得到重现。结合 Trop-2 和 ADAM10 对皮肤、卵巢、结肠、肺和胰腺癌症的预后影响,这些数据表明这种 Trop-2 的激活性裂解在肿瘤的恶性进展中起驱动作用。