Collagens are the most abundant proteins in the body and comprise the basement membranes and stroma through which cancerous invasion occurs; however, a pro-neoplastic function for mutant collagens is undefined. Here we identify COL11A1 mutations in 66 of 100 cutaneous squamous cell carcinomas (cSCCs), the second most common U.S. cancer, concentrated in a triple helical region known to produce trans-dominant collagens. Analysis of COL11A1 and other collagen genes found that they are mutated across common epithelial malignancies. Knockout of mutant COL11A1 impairs cSCC tumorigenesis in vivo. Compared to otherwise genetically identical COL11A1 wild-type tissue, gene-edited mutant COL11A1 skin is characterized by induction of β1 integrin targets and accelerated neoplastic invasion. In mosaic tissue, mutant COL11A1 cells enhanced invasion by neighboring wild-type cells. These results suggest that specific collagens are commonly mutated in cancer and that mutant collagens may accelerate this process.
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http://dx.doi.org/10.1038/s41388-021-02013-y | DOI Listing |
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
May 2024
Graduate Training Base of Jinzhou Medical University, Chaoyang Central Hospital, Chaoyang, Liaoning 122000, China.
Objective: To explore the genetic etiology of a fetus with short limbs identified by prenatal ultrasonography.
Methods: A fetus detected with short limb malformations at Shengjing Hospital Affiliated to China Medical University on October 25, 2021 was selected as the study subject. Prenatal ultrasound and post-abortion imaging were carried out to determine the phenotypic characteristics of the fetus.
Elife
January 2024
Center for Translational Research, Scottish Rite for Children, Dallas, United States.
Adolescent idiopathic scoliosis (AIS) is a common and progressive spinal deformity in children that exhibits striking sexual dimorphism, with girls at more than fivefold greater risk of severe disease compared to boys. Despite its medical impact, the molecular mechanisms that drive AIS are largely unknown. We previously defined a female-specific AIS genetic risk locus in an enhancer near the gene.
View Article and Find Full Text PDFJ Mol Cell Cardiol Plus
December 2023
King's College London, British Heart Foundation Centre of Research Excellence, London, United Kingdom.
Background: Hypertrophic cardiomyopathy (HCM) is an autosomal dominant genetic disorder, characterized by cardiomyocyte hypertrophy, cardiomyocyte disarray and fibrosis, which has a prevalence of ∼1: 200-500 and predisposes individuals to heart failure and sudden death. The mechanisms through which diverse HCM-causing mutations cause cardiac dysfunction remain mostly unknown and their identification may reveal new therapeutic avenues. MicroRNAs (miRNAs) have emerged as critical regulators of gene expression and disease phenotype in various pathologies.
View Article and Find Full Text PDFbioRxiv
November 2023
Center for Pediatric Bone Biology and Translational Research, Scottish Rite for Children, Dallas, TX, USA.
Biochem Biophys Res Commun
October 2022
Henan Provincial People's Hospital, Cerebrovascular Disease Hospital, People's Hospital of Zhengzhou University, Zhengzhou, Henan, 450003, China; Henan Provincial People's Hospital, Cerebrovascular disease hospital, People's Hospital of Henan University, Zhengzhou, Henan, 450003, China; Department of Neurosurgery, The First Hospital of Jilin University, Changchun, Jilin, 130021, China. Electronic address:
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