<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(4)</volume><submitter>Perryman L</submitter><pubmed_abstract>Immunotherapies (such as checkpoint inhibitors) and standard chemotherapies (such as cisplatin) have limitations in the successful treatment of malignant pleural mesothelioma (MPM). Fibrosis is the accumulation of collagen in the extracellular matrix (ECM) of tissues, making them denser than that of healthy tissues and thereby affecting drug delivery and immune cell infiltration. Moreover, fibrosis severely affects the patient's breathing and quality of life. The production of collagen and its assembly is highly regulated by various enzymes such as lysyl oxidases. Many solid tumors aberrantly express the family of lysyl oxidases (LOX/LOXL). This review examines how LOX/LOXLs were found to be dysregulated in noncancerous and cancerous settings, discusses their roles in solid tumor fibrosis </pubmed_abstract><journal>Cancers</journal><pagination>981</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8870010</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Fibrosis in Mesothelioma: Potential Role of Lysyl Oxidases.</pubmed_title><pmcid>PMC8870010</pmcid><pubmed_authors>Gray SG</pubmed_authors><pubmed_authors>Perryman L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fibrosis in Mesothelioma: Potential Role of Lysyl Oxidases.</name><description>Immunotherapies (such as checkpoint inhibitors) and standard chemotherapies (such as cisplatin) have limitations in the successful treatment of malignant pleural mesothelioma (MPM). Fibrosis is the accumulation of collagen in the extracellular matrix (ECM) of tissues, making them denser than that of healthy tissues and thereby affecting drug delivery and immune cell infiltration. Moreover, fibrosis severely affects the patient's breathing and quality of life. The production of collagen and its assembly is highly regulated by various enzymes such as lysyl oxidases. Many solid tumors aberrantly express the family of lysyl oxidases (LOX/LOXL). This review examines how LOX/LOXLs were found to be dysregulated in noncancerous and cancerous settings, discusses their roles in solid tumor fibrosis </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-18T12:09:53.891Z</modification><creation>2025-04-06T21:49:48.509Z</creation></dates><accession>S-EPMC8870010</accession><cross_references><pubmed>35205728</pubmed><doi>10.3390/cancers14040981</doi></cross_references></HashMap>