Advances in Translational Research for Soft Tissue Sarcomas

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Biomarkers".

Deadline for manuscript submissions: closed (15 November 2023) | Viewed by 3480

Special Issue Editors


E-Mail Website
Guest Editor
Department of Health Science, University of Florence, Largo Brambilla 3, 50134 Florence, Italy
Interests: bone tumors; soft tissue sarcomas; orthopaedic oncology; orthopaedic surgery; osteoarticular reconstructions

E-Mail Website
Guest Editor
Medical Oncology Unit, Careggi University Hospital, Largo Brambilla 3, 50134 Florence, Italy
Interests: biomarkers; epigenetic; liquid biopsy; molecular biology; omics; chemoresistance

E-Mail Website
Guest Editor
Department of Orthopaedic Oncology, Careggi University Hospital, Largo Brambilla 3, 50134 Florence, Italy
Interests: bone tumors; soft tissue sarcomas; orthopaedic oncology; orthopaedic surgery; osteoarticular reconstructions

Special Issue Information

Dear Colleagues,

Soft tissue sarcomas (STSs) are rare and heterogeneous tumors of mesenchymal origin, presenting with an incidence around 50–60 new cases per year for every million people. Around 30–40% of localized STS will finally develop metastases, highlighting how the efficacy of our treatments requires improvement. The difficulty in the development of new therapeutic strategies is enhanced by the complexity and heterogeneity of STS, which are, at the moment, subclassified into more than 70 histological and molecular types with varying biology, molecular aberrations, clinical behaviours, and with a trend to a progressive addition of new subtypes as molecular and genetics data about these tumors are obtained by researchers. In localized disease, surgery remains the mainstay of treatment of STS, often combined with radiotherapy. For locally advanced or metastatic STS, the therapeutic options are limited, and clinical responses to chemotherapy are variable and usually scarce, with good responses to anticancer therapies continuing to be limited to a small subset of STS patients. In this scenario, it is urgently needed to broaden the knowledge of heterogeneous molecular patterns of STSs to understand the activable pathways that define the prognosis and underly the risk of relapse. Thus, a translational research approach, with the aim to join the efforts of clinical physicians and basic researchers, is of utmost importance to detect biomarkers that can predict drug response and to explain the differences in treatment efficacy and toxicity among patients.

This Special Issue of Cancers will focus on novel prognostic and predictive markers, as well as novel approaches in addressing and monitoring STS patients, in order to improve our understanding of these tumors and the efficacy of our therapeutical strategies.

Prof. Dr. Domenico Andrea Campanacci
Dr. Serena Pillozzi
Dr. Guido Scoccianti
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • chemoresistance
  • liquid biopsy
  • soft tissue sarcoma
  • molecular biology
  • predictive and prognostic biomarker
  • pharmacogenetic

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

19 pages, 9446 KiB  
Article
ERK5 Is a Major Determinant of Chemical Sarcomagenesis: Implications in Human Pathology
by Elena Arconada-Luque, Jaime Jiménez-Suarez, Raquel Pascual-Serra, Syong Hyun Nam-Cha, Teresa Moline, Francisco J. Cimas, Germán Fliquete, Marta Ortega-Muelas, Olga Roche, Diego M. Fernández-Aroca, Raúl Muñoz Velasco, Natalia García-Flores, Cristina Garnés-García, Adrián Sánchez-Fdez, Sofía Matilla-Almazán, Víctor J. Sánchez-Arévalo Lobo, Javier Hernández-Losa, Borja Belandia, Atanasio Pandiella, Azucena Esparís-Ogando, Santiago Ramón y Cajal, Luis del Peso, Ricardo Sánchez-Prieto and María José Ruiz-Hidalgoadd Show full author list remove Hide full author list
Cancers 2022, 14(14), 3509; https://0-doi-org.brum.beds.ac.uk/10.3390/cancers14143509 - 19 Jul 2022
Cited by 2 | Viewed by 3051
Abstract
Sarcomas are a heterogeneous group of tumors in which the role of ERK5 is poorly studied. To clarify the role of this MAPK in sarcomatous pathology, we used a murine 3-methyl-cholanthrene (3MC)-induced sarcoma model. Our data show that 3MC induces pleomorphic sarcomas with [...] Read more.
Sarcomas are a heterogeneous group of tumors in which the role of ERK5 is poorly studied. To clarify the role of this MAPK in sarcomatous pathology, we used a murine 3-methyl-cholanthrene (3MC)-induced sarcoma model. Our data show that 3MC induces pleomorphic sarcomas with muscle differentiation, showing an increased expression of ERK5. Indeed, this upregulation was also observed in human sarcomas of muscular origin, such as leiomyosarcoma or rhabdomyosarcoma. Moreover, in cell lines derived from these 3MC-induced tumors, abrogation of Mapk7 expression by using specific shRNAs decreased in vitro growth and colony-forming capacity and led to a marked loss of tumor growth in vivo. In fact, transcriptomic profiling in ERK5 abrogated cell lines by RNAseq showed a deregulated gene expression pattern for key biological processes such as angiogenesis, migration, motility, etc., correlating with a better prognostic in human pathology. Finally, among the various differentially expressed genes, Klf2 is a key mediator of the biological effects of ERK5 as indicated by its specific interference, demonstrating that the ERK5–KLF2 axis is an important determinant of sarcoma biology that should be further studied in human pathology. Full article
(This article belongs to the Special Issue Advances in Translational Research for Soft Tissue Sarcomas)
Show Figures

Figure 1

Back to TopTop