Namkoong Hong, Shin Seung Min, Kim Hyun Kee, Ha Seon-Ah, Cho Goang Won, Hur Soo Young, Kim Tae Eung, Kim Jin Woo
Molecular Genetic Laboratory, College of Medicine, The Catholic University of Korea, Seoul 137-040, Korea.
BMC Cancer. 2006 Mar 18;6:74. doi: 10.1186/1471-2407-6-74.
Basic studies of oncogenesis have demonstrated that either the elevated production of particular oncogene proteins or the occurrence of qualitative abnormalities in oncogenes can contribute to neoplastic cellular transformation. The purpose of our study was to identify an unique gene that shows cancer-associated expression, and characterizes its function related to human carcinogenesis.
We used the differential display (DD) RT-PCR method using normal cervical, cervical cancer, metastatic cervical tissues, and cervical cancer cell lines to identify genes overexpressed in cervical cancers and identified gremlin 1 which was overexpressed in cervical cancers. We determined expression levels of gremlin 1 using Northern blot analysis and immunohistochemical study in various types of human normal and cancer tissues. To understand the tumorigenesis pathway of identified gremlin 1 protein, we performed a yeast two-hybrid screen, GST pull down assay, and immunoprecipitation to identify gremlin 1 interacting proteins.
DDRT-PCR analysis revealed that gremlin 1 was overexpressed in uterine cervical cancer. We also identified a human gremlin 1 that was overexpressed in various human tumors including carcinomas of the lung, ovary, kidney, breast, colon, pancreas, and sarcoma. PIG-2-transfected HEK 293 cells exhibited growth stimulation and increased telomerase activity. Gremlin 1 interacted with homo sapiens tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide (14-3-3 eta; YWHAH). YWHAH protein binding site for gremlin 1 was located between residues 61-80 and gremlin 1 binding site for YWHAH was found to be located between residues 1 to 67.
Gremlin 1 may play an oncogenic role especially in carcinomas of the uterine cervix, lung, ovary, kidney, breast, colon, pancreas, and sarcoma. Over-expressed gremlin 1 functions by interaction with YWHAH. Therefore, Gremlin 1 and its binding protein YWHAH could be good targets for developing diagnostic and therapeutic strategies against human cancers.
肿瘤发生的基础研究表明,特定癌基因蛋白的产量升高或癌基因中出现定性异常都可能导致肿瘤细胞转化。我们研究的目的是鉴定一个显示与癌症相关表达的独特基因,并表征其与人类致癌作用相关的功能。
我们使用差异显示(DD)RT-PCR方法,利用正常宫颈组织、宫颈癌组织、转移性宫颈组织和宫颈癌细胞系来鉴定在宫颈癌中过表达的基因,并鉴定出在宫颈癌中过表达的gremlin 1。我们通过Northern印迹分析和免疫组织化学研究,测定了gremlin 1在各种类型的人类正常组织和癌组织中的表达水平。为了了解已鉴定的gremlin 1蛋白的肿瘤发生途径,我们进行了酵母双杂交筛选、GST下拉分析和免疫沉淀,以鉴定与gremlin 1相互作用的蛋白。
DDRT-PCR分析显示gremlin 1在子宫颈癌中过表达。我们还鉴定出一种人类gremlin 1,它在包括肺癌、卵巢癌、肾癌、乳腺癌、结肠癌、胰腺癌和肉瘤在内的各种人类肿瘤中过表达。用PIG-2转染的HEK 293细胞表现出生长刺激和端粒酶活性增加。Gremlin 1与人类酪氨酸3-单加氧酶/色氨酸5-单加氧酶激活蛋白η多肽(14-3-3 eta;YWHAH)相互作用。Gremlin 1的YWHAH蛋白结合位点位于第61-80位氨基酸残基之间,而YWHAH的gremlin 1结合位点位于第1-67位氨基酸残基之间。
Gremlin 1可能尤其在子宫颈癌、肺癌、卵巢癌、肾癌、乳腺癌、结肠癌、胰腺癌和肉瘤中发挥致癌作用。过表达的gremlin 1通过与YWHAH相互作用发挥功能。因此,Gremlin 1及其结合蛋白YWHAH可能是开发针对人类癌症的诊断和治疗策略的良好靶点。