Affiliations: [a] Technology of Medical Laboratory Department, College of Applied Health Science Technology, Misr University for Science and Technology, 6th of October, Egypt | [b] Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA | [c] Division of Gastroenterology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA
Correspondence:
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Corresponding author: Ayman Mohamed Metwally, Technology of Medical Laboratory Department, College of Applied Health Science Technology, Misr University for Science and Technology, Almotamayez District, 6th October, 77, Egypt. Tel.: +20 100 549 8680; E-mail: [email protected],ayman_doctor@hotmail.%****␣cbm-32-cbm203121_temp.tex␣Line␣25␣****com.
Abstract: BACKGROUND: Recent studies demonstrated the involvement of mesenchymal stem/stromal cells (MSCs) in carcinogenesis, but the molecular mechanism behind this transformation is still obscured. OBJECTIVE: To screen both the expression levels of polycomb and trithorax epigenetic regulators and TrP53 mutations in early and late MSC culture passages in an attempt to decipher the mechanism of spontaneous transformation. METHODS: The study was conducted on early and late passages of MSC culture model from C57BL/6J mice. The expression profile of 84 epigenetic regulators was examined using RT2 profiler PCR array. TrP53 mutations in the DNA binding domain was screened. Codons, amino acids positions and the corresponding human variants were detected in P53 sequences. RESULTS: Sixty-two epigenetic regulators were dysregulated. Abnormalities were detected starting the third passage. Nine regulators were dysregulated in all passages. (C>G) substitution P53 mutation was detected in passage 3 resulting in Ser152Arg substitution. Passages 6, 9, 12 and the last passage showed T>C substitution resulting in Cys235Arg substitution. The last passage had T deletion and A insertion resulting in frame shift mutations changing the p.Phe286Ser and p.Asn103Lys respectively. CONCLUSION: In vitro expanded MSCs undergo transformation through alteration of epigenetic regulators which results in genomic instability and frequent P53 mutations.
