Literature DB >> 27528700

Recurrent TRIO Fusion in Nontranslocation-Related Sarcomas.

Lucile Delespaul1,2, Tom Lesluyes1,2, Gaëlle Pérot1,3, Céline Brulard1, Lydia Lartigue1,2, Jessica Baud1,2, Pauline Lagarde1, Sophie Le Guellec4, Agnès Neuville1,3, Philippe Terrier5, Dominique Vince-Ranchère6, Susanne Schmidt7, Anne Debant7, Jean-Michel Coindre1,2,3, Frédéric Chibon8,3.   

Abstract

PURPOSE: Despite various differences, nontranslocation-related sarcomas (e.g., comprising undifferentiated pleomorphic sarcoma, leiomyosarcoma, myxofibrosarcoma) are unified by their complex genetics. Extensive analysis of the tumor genome using molecular cytogenetic approaches showed many chromosomal gains, losses, and translocations per cell. Genomic quantitative alterations and expression variations have been extensively studied by adapted high-throughput approaches, yet translocations still remained unscreened. We therefore analyzed 117 nontranslocation-related sarcomas by RNA sequencing to identify fusion genes. EXPERIMENTAL
DESIGN: We performed RNA sequencing and applied a bioinformatics pipeline dedicated to the detection of fusion transcripts. RT-PCR and Sanger sequencing were then applied to validate predictions and to search for recurrence and specificity.
RESULTS: Among the 6,772 predicted fusion genes, 420 were in-frame. One recurrent rearrangement, consistently involving TRIO with various partners, was identified in 5.1% of cases. TRIO translocations are either intrachromosomal with TERT or interchromosomal with LINC01504 or ZNF558 Our results suggest that all translocations led to a truncated TRIO protein either directly or indirectly by alternative splicing. TRIO rearrangement is associated with a modified transcriptomic program to immunity/inflammation, proliferation and migration, and an increase in proliferation.
CONCLUSIONS: TRIO fusions have been identified in four different sarcoma histotypes, likely meaning that they are not related to a primary oncogenic event but rather to a secondary one implicated in tumor progression. Moreover, they appear to be specific to nontranslocation-related sarcomas, as no such rearrangement was identified in sarcomas with simple genetics. More cases could lead to a significant association of these fusions to a specific clinical behavior. Clin Cancer Res; 23(3); 857-67. ©2016 AACR. ©2016 American Association for Cancer Research.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27528700     DOI: 10.1158/1078-0432.CCR-16-0290

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  13 in total

1.  Identification of Novel Fusion Transcripts in Undifferentiated Pleomorphic Sarcomas by Transcriptome Sequencing.

Authors:  Biqiang Zheng; Shuirong Zhang; Weiluo Cai; Jian Wang; Ting Wang; Ning Tang; Yingqiang Shi; Xiaoying Luo; Wangjun Yan
Journal:  Cancer Genomics Proteomics       Date:  2019 Sep-Oct       Impact factor: 4.069

Review 2.  Biology and Management of Undifferentiated Pleomorphic Sarcoma, Myxofibrosarcoma, and Malignant Peripheral Nerve Sheath Tumors: State of the Art and Perspectives.

Authors:  Brigitte C Widemann; Antoine Italiano
Journal:  J Clin Oncol       Date:  2017-12-08       Impact factor: 44.544

Review 3.  Angiofibroma of soft tissue: Current status of pathology and genetics.

Authors:  Shizuhide Nakayama; Jun Nishio; Mikiko Aoki; Kaori Koga; Kazuki Nabeshima; Takuaki Yamamoto
Journal:  Histol Histopathol       Date:  2022-02-25       Impact factor: 2.130

4.  Germinal GLT8D1, GATAD2A and SLC25A39 mutations in a patient with a glomangiopericytal tumor and five different sarcomas over a 10-year period.

Authors:  Arnaud Beddok; Gaëlle Pérot; Sophie Le Guellec; Noémie Thebault; Alexandre Coutte; Henri Sevestre; Bruno Chauffert; Frédéric Chibon
Journal:  Sci Rep       Date:  2021-05-07       Impact factor: 4.379

5.  Non-coding RNAs in cancers with chromosomal rearrangements: the signatures, causes, functions and implications.

Authors:  Cai Han; Lin-Yu Sun; Wen-Tao Wang; Yu-Meng Sun; Yue-Qin Chen
Journal:  J Mol Cell Biol       Date:  2019-10-25       Impact factor: 6.216

6.  Cell-cell fusion of mesenchymal cells with distinct differentiations triggers genomic and transcriptomic remodelling toward tumour aggressiveness.

Authors:  Lucile Delespaul; Caroline Gélabert; Tom Lesluyes; Sophie Le Guellec; Gaëlle Pérot; Laura Leroy; Jessica Baud; Candice Merle; Lydia Lartigue; Frédéric Chibon
Journal:  Sci Rep       Date:  2020-12-10       Impact factor: 4.379

7.  Systematic Transcriptome Analysis Reveals the Inhibitory Function of Cinnamaldehyde in Non-Small Cell Lung Cancer.

Authors:  Ru Chen; Juan Wu; Chang Lu; Ting Yan; Yu Qian; Huiqing Shen; Yujing Zhao; Jianzhen Wang; Pengzhou Kong; Xinri Zhang
Journal:  Front Pharmacol       Date:  2021-02-09       Impact factor: 5.810

8.  The Immunosuppressive Niche of Soft-Tissue Sarcomas is Sustained by Tumor-Associated Macrophages and Characterized by Intratumoral Tertiary Lymphoid Structures.

Authors:  Lingling Chen; Teniola Oke; Nicholas Siegel; Gady Cojocaru; Ada J Tam; Richard L Blosser; Jessica Swailes; John A Ligon; Andriana Lebid; Carol Morris; Adam Levin; Daniel S Rhee; Fabian M Johnston; Jonathan B Greer; Christian F Meyer; Brian H Ladle; Elizabeth D Thompson; Elizabeth A Montgomery; Woonyoung Choi; David J McConkey; Robert A Anders; Drew M Pardoll; Nicolas J Llosa
Journal:  Clin Cancer Res       Date:  2020-04-24       Impact factor: 12.531

9.  Integrated genetic and epigenetic analysis of myxofibrosarcoma.

Authors:  Koichi Ogura; Fumie Hosoda; Yasuhito Arai; Hiromi Nakamura; Natsuko Hama; Yasushi Totoki; Akihiko Yoshida; Momoko Nagai; Mamoru Kato; Erika Arakawa; Wakako Mukai; Hirofumi Rokutan; Akira Kawai; Sakae Tanaka; Tatsuhiro Shibata
Journal:  Nat Commun       Date:  2018-07-17       Impact factor: 14.919

10.  Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas.

Authors: 
Journal:  Cell       Date:  2017-11-02       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.