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      Ovine Pulmonary Adenocarcinoma: A Unique Model to Improve Lung Cancer Research

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          Abstract

          Lung cancer represents a major worldwide health concern; although advances in patient management have improved outcomes for some patients, overall 5-year survival rates are only around 15%. In vitro studies and mouse models are commonly used to study lung cancer and their use has increased the molecular understanding of the disease. Unfortunately, mouse models are poor predictors of clinical outcome and seldom mimic advanced stages of the human disease. Animal models that more accurately reflect human disease are required for progress to be made in improving treatment outcomes and prognosis. Similarities in pulmonary anatomy and physiology potentially make sheep better models for studying human lung function and disease. Ovine pulmonary adenocarcinoma (OPA) is a naturally occurring lung cancer that is caused by the jaagsiekte sheep retrovirus. The disease is endemic in many countries throughout the world and has several features in common with human lung adenocarcinomas, including histological classification and activation of common cellular signaling pathways. Here we discuss the in vivo and in vitro OPA models that are currently available and describe the advantages of using pre-clinical naturally occurring OPA cases as a translational animal model for human lung adenocarcinoma. The challenges and options for obtaining these OPA cases for research purposes, along with their use in developing novel techniques for the evaluation of chemotherapeutic agents or for monitoring the tumor microenvironment in response to treatment, are also discussed.

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          Most cited references105

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          SH2 domains recognize specific phosphopeptide sequences.

          A phosphopeptide library was used to determine the sequence specificity of the peptide-binding sites of SH2 domains. One group of SH2 domains (Src, Fyn, Lck, Fgr, Abl, Crk, and Nck) preferred sequences with the general motif pTyr-hydrophilic-hydrophilic-Ile/Pro while another group (SH2 domains of p85, phospholipase C-gamma, and SHPTP2) selected the general motif pTyr-hydrophobic-X-hydrophobic. Individual members of these groups selected unique sequences, except the Src subfamily (Src, Fyn, Lck, and Fgr), which all selected the sequence pTyr-Glu-Glu-Ile. The variability in SH2 domain sequences at likely sites of contact provides a structural basis for the phosphopeptide selectivity of these families. Possible in vivo binding sites of the SH2 domains are discussed.
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            Animal models of human respiratory syncytial virus disease.

            Infection with the human pneumovirus pathogen, respiratory syncytial virus (hRSV), causes a wide spectrum of respiratory disease, notably among infants and the elderly. Laboratory animal studies permit detailed experimental modeling of hRSV disease and are therefore indispensable in the search for novel therapies and preventative strategies. Present animal models include several target species for hRSV, including chimpanzees, cattle, sheep, cotton rats, and mice, as well as alternative animal pneumovirus models, such as bovine RSV and pneumonia virus of mice. These diverse animal models reproduce different features of hRSV disease, and their utilization should therefore be based on the scientific hypothesis under investigation. The purpose of this review is to summarize the strengths and limitations of each of these animal models. Our intent is to provide a resource for investigators and an impetus for future research.
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              Identification of cancer initiating cells in K-Ras driven lung adenocarcinoma.

              Ubiquitous expression of a resident K-Ras(G12V) oncogene in adult mice revealed that most tissues are resistant to K-Ras oncogenic signals. Indeed, K-Ras(G12V) expression only induced overt tumors in lungs. To identify these transformation-permissive cells, we induced K-Ras(G12V) expression in a very limited number of adult lung cells (0.2%) and monitored their fate by X-Gal staining, a surrogate marker coexpressed with the K-Ras(G12V) oncoprotein. Four weeks later, 30% of these cells had proliferated to form small clusters. However, only SPC(+) alveolar type II (ATII) cells were able to form hyperplastic lesions, some of which progressed to adenomas and adenocarcinomas. In contrast, induction of K-Ras(G12V) expression in lung cells by intratracheal infection with adenoviral-Cre particles generated hyperplasias in all regions except the proximal airways. Bronchiolar and bronchioalveolar duct junction hyperplasias were primarily made of CC10(+) Clara cells. Some of them progressed to form benign adenomas. However, only alveolar hyperplasias, exclusively made up of SPC(+) ATII cells, progressed to yield malignant adenocarcinomas. Adenoviral infection induced inflammatory infiltrates primarily made of T and B cells. This inflammatory response was essential for the development of K-Ras(G12V)-driven bronchiolar hyperplasias and adenomas, but not for the generation of SPC(+) ATII lesions. Finally, activation of K-Ras(G12V) during embryonic development under the control of a Sca1 promoter yielded CC10(+), but not SPC(+), hyperplasias, and adenomas. These results, taken together, illustrate that different types of lung cells can generate benign lesions in response to K-Ras oncogenic signals. However, in adult mice, only SPC(+) ATII cells were able to yield malignant adenocarcinomas.
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                Author and article information

                Contributors
                Journal
                Front Oncol
                Front Oncol
                Front. Oncol.
                Frontiers in Oncology
                Frontiers Media S.A.
                2234-943X
                26 April 2019
                2019
                : 9
                : 335
                Affiliations
                [1] 1The Royal (Dick) School of Veterinary Studies and Roslin Institute, University of Edinburgh , Edinburgh, United Kingdom
                [2] 2Cancer Research UK Edinburgh Centre and Division of Pathology Laboratories, Institute of Genetics and Molecular Medicine, University of Edinburgh , Edinburgh, United Kingdom
                [3] 3School of Engineering and Physical Sciences, Institute of Sensors, Signals and Systems, Heriot-Watt University , Edinburgh, United Kingdom
                [4] 4School of Engineering, Institute for Integrated Micro and Nano Systems, The King's Buildings , Edinburgh, United Kingdom
                [5] 5Moredun Research Institute, Pentlands Science Park , Midlothian, United Kingdom
                Author notes

                Edited by: Kyle Schachtschneider, University of Illinois at Chicago, United States

                Reviewed by: Massimo Palmarini, MRC-University of Glasgow Centre For Virus Research (MRC), United Kingdom; Ramon A. Juste, Servicio Regional de Investigación y Desarrollo Agroalimentario (SERIDA), Spain

                *Correspondence: Mark E. Gray s9900757@ 123456sms.ed.ac.uk

                This article was submitted to Molecular and Cellular Oncology, a section of the journal Frontiers in Oncology

                Article
                10.3389/fonc.2019.00335
                6498990
                31106157
                193e502e-3301-4106-9e56-a1e8a68b097c
                Copyright © 2019 Gray, Meehan, Sullivan, Marland, Greenhalgh, Gregson, Clutton, Ward, Cousens, Griffiths, Murray and Argyle.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 14 February 2019
                : 11 April 2019
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 113, Pages: 11, Words: 8928
                Funding
                Funded by: Engineering and Physical Sciences Research Council 10.13039/501100000266
                Funded by: Wellcome Trust 10.13039/100004440
                Funded by: Rural and Environment Science and Analytical Services Division 10.13039/100011310
                Categories
                Oncology
                Review

                Oncology & Radiotherapy
                human lung cancer,jaagsiekte sheep retrovirus,ovine pulmonary adenocarcinoma,sheep lung cancer models,comparative oncology

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