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A Novel Notch-YAP Circuit Drives Stemness and Tumorigenesis in Embryonal Rhabdomyosarcoma.一种新型 Notch-YAP 通路驱动胚胎性横纹肌肉瘤的干性和肿瘤发生。
Mol Cancer Res. 2017 Dec;15(12):1777-1791. doi: 10.1158/1541-7786.MCR-17-0004. Epub 2017 Sep 18.
2
Update on molecular findings in rhabdomyosarcoma.横纹肌肉瘤分子研究结果的最新进展。
Pathology. 2017 Apr;49(3):238-246. doi: 10.1016/j.pathol.2016.12.345. Epub 2017 Feb 27.
3
The Hippo Pathway: A Master Regulatory Network Important in Development and Dysregulated in Disease.河马通路:一个在发育过程中起重要作用且在疾病中失调的主要调控网络。
Curr Top Dev Biol. 2017;123:181-228. doi: 10.1016/bs.ctdb.2016.12.001. Epub 2017 Jan 19.
4
Pediatric soft tissue tumor pathology: A happy morpho-molecular union.儿科软组织肿瘤病理学:形态学与分子学的美满结合。
Semin Diagn Pathol. 2016 Nov;33(6):377-395. doi: 10.1053/j.semdp.2016.08.008. Epub 2016 Sep 5.
5
TAZ and YAP are frequently activated oncoproteins in sarcomas.TAZ和YAP是肉瘤中经常被激活的癌蛋白。
Oncotarget. 2016 May 24;7(21):30094-108. doi: 10.18632/oncotarget.8979.
6
Role of the YAP Oncoprotein in Priming Ras-Driven Rhabdomyosarcoma.Yes相关蛋白癌蛋白在启动Ras驱动的横纹肌肉瘤中的作用。
PLoS One. 2015 Oct 23;10(10):e0140781. doi: 10.1371/journal.pone.0140781. eCollection 2015.
7
The Role of Immunohistochemistry in Rhabdomyosarcoma Diagnosis Using Tissue Microarray Technology and a Xenograft Model.免疫组织化学在横纹肌肉瘤诊断中的作用:应用组织芯片技术和异种移植模型
Fetal Pediatr Pathol. 2015;34(5):271-81. doi: 10.3109/15513815.2015.1042604. Epub 2015 Jun 30.
8
The Hippo signal transduction pathway in soft tissue sarcomas.软组织肉瘤中的河马信号转导通路。
Biochim Biophys Acta. 2015 Aug;1856(1):121-9. doi: 10.1016/j.bbcan.2015.05.006. Epub 2015 Jun 4.
9
The Hippo transducer YAP1 transforms activated satellite cells and is a potent effector of embryonal rhabdomyosarcoma formation.Hippo 信号转导蛋白 YAP1 可激活卫星细胞,并可作为胚胎性横纹肌肉瘤形成的有效效应因子。
Cancer Cell. 2014 Aug 11;26(2):273-87. doi: 10.1016/j.ccr.2014.05.029. Epub 2014 Jul 31.
10
Elevated YAP and its downstream targets CCN1 and CCN2 in basal cell carcinoma: impact on keratinocyte proliferation and stromal cell activation.基底细胞癌中 YAP 及其下游靶标 CCN1 和 CCN2 的上调:对角质形成细胞增殖和基质细胞激活的影响。
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YAP 染色在横纹肌肉瘤中的潜在价值。

Potential Value of YAP Staining in Rhabdomyosarcoma.

机构信息

Division of Anatomic Pathology, Children's Mercy Hospital, University of Missouri-Kansas City, Kansas City, Missouri.

Division of Health Services and Outcomes Research, Children's Mercy Hospital, University of Missouri-Kansas City, Kansas City, Missouri.

出版信息

J Histochem Cytochem. 2018 Aug;66(8):577-584. doi: 10.1369/0022155418766515. Epub 2018 Mar 29.

DOI:10.1369/0022155418766515
PMID:29596030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6071181/
Abstract

Rhabdomyosarcoma (RMS) is a common malignancy of soft tissue, subclassified as alveolar (ARMS), pleomorphic (PRMS), spindle cell/sclerosing (SRMS), and embryonal (ERMS) types. The Yes-associated protein (YAP) is a member of the Hippo pathway and a transcriptional regulator that controls cell proliferation. We have studied the immunohistochemical expression of YAP in different RMSs, arranged in tissue microarray (TMA) and whole slide formats. Pertinent clinical data including patient age, gender, tumor location, and clinical stage were collected. Out of 96 TMA cases, 30 cases (31%) were pleomorphic, 27 (28%) were embryonal, 24 (25%) alveolar, and 15 (16%) spindle cell. Positive nuclear YAP staining was seen in the PRMS (17/30, 56.7%), SRMS (7/15, 46.7%), ERMS (19/27 or 70%), and less in ARMS (37.5%). YAP nuclear staining was significantly more prevalent in ERMS than ARMS ( p=0.02). Of the 41 whole slide cases, nuclear staining was detected in all ARMS but was restricted in distribution to <30% of the cells, in contrast to ERMS and SRMS, which had diffuse or >30% staining. These results highlight the role of YAP in RMS tumorigenesis, a fact that can be useful in engineering targeted therapy. Restricted nuclear YAP staining (<30% of cells) may be of value in the diagnosis of ARMS.

摘要

横纹肌肉瘤(RMS)是一种常见的软组织恶性肿瘤,分为腺泡型(ARMS)、多形性(PRMS)、梭形细胞/硬化型(SRMS)和胚胎型(ERMS)。Yes 相关蛋白(YAP)是 Hippo 通路的一个成员,是一种转录调控因子,控制细胞增殖。我们研究了不同 RMS 中 YAP 的免疫组织化学表达,以组织微阵列(TMA)和全玻片格式排列。收集了包括患者年龄、性别、肿瘤位置和临床分期在内的相关临床数据。在 96 例 TMA 病例中,30 例(31%)为多形性,27 例(28%)为胚胎性,24 例(25%)为腺泡型,15 例(16%)为梭形细胞。PRMS(17/30,56.7%)、SRMS(7/15,46.7%)、ERMS(19/27 或 70%)可见核 YAP 染色阳性,而 ARMS 阳性率较低(37.5%)。YAP 核染色在 ERMS 中比 ARMS 更为常见(p=0.02)。在 41 例全玻片病例中,所有 ARMS 均检测到核染色,但仅限于<30%的细胞分布,而 ERMS 和 SRMS 则呈弥漫性或>30%的染色。这些结果突出了 YAP 在 RMS 肿瘤发生中的作用,这一事实可能有助于设计靶向治疗。核 YAP 染色受限(<30%的细胞)可能对 ARMS 的诊断有价值。