摘要
在卵巢上皮癌(EOC)中,MIS通路是潜在的治疗靶点:信号通路需要II型(T2R)和I型受体(1R),最后会导致生长抑制。MISR2在卵巢上皮癌中有表达,但是候选型T1R的患病率和相对贡献率仍然是未知的。我们想要:a)确定卵巢上皮癌中T1R的表达;b)评估T1R在临床试验中表达的影响;c)验证MIS依赖Smad信号通路以及 在原发性卵巢癌细胞的生长抑制。 组织微阵列(TMA)被开发用于分析T1Rs (ALK2/3/6)和 MISR2的表达。原代细胞培养源于曾经特定对MIS有反应的术后腹水。 在311例原发癌的TMA中,最常见的受体组合被证明是: MISR2+/ALK2+3+6+ (36%); MISR2+/ALK2+3+6- (34%); MISR2-/ALK2+3+6- (18%); 和MISR2-/ALK2+3+6+ (6.8%)。组合之间总存活率是无差异的。 ALK6受体是在T1R中表达最少的,在疾病早期还和低存活率正相关 (p =0.03)。大多数原代细胞培养表达 MISR2 (14/22 (63.6%)):它们中的95%表达ALK 2 和ALK3,然而54.5%表达ALK6。 MIS依赖 Smad磷酸化被观察到是培养中最多的(75%)。用MIS的治疗导致细胞活力在原代培养中降低到平均71% (范围: 57-87%)。MIS信号通路依赖于 MISR2 和特定T1R的存在。卵巢上皮癌中的大多数T1R目前存在MIS依赖信号,这样的细胞也证明对MIS有恰当的反应。
关键词: ALK2, ALK3,ALK6,苗勒管抑制物质,卵巢癌。
Current Molecular Medicine
Title:Patterns of Müllerian Inhibiting Substance Type II and Candidate Type I Receptors in Epithelial Ovarian Cancer†
Volume: 16 Issue: 3
Author(s): E. Basal, T. Ayeni, Q. Zhang, C. Langstraat, P.K. Donahoe, D. Pepin, X. Yin, E. Leof and W. Cliby
Affiliation:
关键词: ALK2, ALK3,ALK6,苗勒管抑制物质,卵巢癌。
摘要: The MIS pathway is a potential therapeutic target in epithelial ovarian cancer (EOC): signaling requires both type II (T2R) and type I receptors (T1R), and results in growth inhibition. MISR2 is expressed in EOC, but the prevalence and relative contributions of candidate T1R remain unknown. We sought to: a) determine expression of T1R in EOC; b) assess impact of T1R expression with clinical outcomes; c) verify MIS-dependent Smad signaling and growth inhibition in primary EOC cell cultures.
Tissue microarrays (TMA) were developed for analysis of T1Rs (ALK2/3/6) and MISR2 expression. Primary cell cultures were initiated from ascites harvested at surgery which were used to characterize response to MIS.
TMA’s from 311 primary cancers demonstrated the most common receptor combinations were: MISR2+/ALK2+3+6+ (36%); MISR2+/ALK2+3+6- (34%); MISR2-/ALK2+3+6- (18%); and MISR2-/ALK2+3+6+ (6.8%). No differences in overall survival (OS) were noted between combinations. The ALK6 receptor was least often expressed T1R and was associated with lower OS in early stage disease only (p =0.03). Most primary cell cultures expressed MISR2 (14/22 (63.6%)): 95% of these express ALK 2 and ALK3, whereas 54.5% expressed ALK6. MIS-dependent Smad phosphorylation was seen in the majority of cultures (75%). Treatment with MIS led to reduced cell viability at an average of 71% (range: 57-87%) in primary cultures. MIS signaling is dependent upon the presence of both MISR2 and specific T1R. In the majority of EOC, the T1R required for MIS-dependent signaling are present and such cells demonstrate appropriate response to MIS.
Export Options
About this article
Cite this article as:
E. Basal, T. Ayeni, Q. Zhang, C. Langstraat, P.K. Donahoe, D. Pepin, X. Yin, E. Leof and W. Cliby , Patterns of Müllerian Inhibiting Substance Type II and Candidate Type I Receptors in Epithelial Ovarian Cancer†, Current Molecular Medicine 2016; 16 (3) . https://dx.doi.org/10.2174/1566524016666160225151131
DOI https://dx.doi.org/10.2174/1566524016666160225151131 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers