Literature DB >> 23679560

Prognostic role of immunohistochemical analysis of 5 mc in myelodysplastic syndromes.

Antonella Poloni1, Gaia Goteri2, Antonio Zizzi2, Federica Serrani1, Silvia Trappolini1, Benedetta Costantini1, Marianna Mariani1, Attilio Olivieri1, Massimo Catarini3, Riccardo Centurioni4, Francesco Alesiani5, Federica Giantomassi2, Daniela Stramazzotti2, Simona Biagetti2, Simona Alfonsi2, Eleonora Berardinelli1, Pietro Leoni1.   

Abstract

BACKGROUND: Aberrant DNA methylation at CpG islands within promoters is increasingly recognised as a common event in human cancers and has been associated with the silencing of important tumour suppressor genes. Epigenetic therapy using hypomethylating agents has demonstrated clinical effectiveness; the drugs azacitidine and decitabine have been approved for the treatment of MDS.
METHOD: We investigated the association between global DNA methylation and clinical outcome in MDS. We evaluated 134 MDS bone marrow trephine biopsies (BMTB) by immunohistochemistry and compared the results with those from an age-matched group of normal BMTB. Immunohistochemistry was performed on paraffin-embedded sections using the anti-5-methylcytosine (5mc) antibody.
RESULTS: Our results showed that the 5mc immunostaining score (M-score) of patients with MDS was higher than those of normal controls and that overall survival significantly correlated with global DNA methylation, age and IPSS score. Therefore, we found that patients with high levels of methylation had a shorter median overall survival (OS) compared with patients with lower levels. These immunohistochemistry results were confirmed by analysing global DNA methylation on LINE-1 sequences using the COBRA method and pyrosequencing.
CONCLUSION: This study reports that global DNA methylation detected by immunohistochemistry predicts OS in MDS.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  DNA methylation; hypomethylating agents; immunohistochemistry; myelodysplastic syndromes; pyrosequencing

Mesh:

Substances:

Year:  2013        PMID: 23679560     DOI: 10.1111/ejh.12145

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   3.674


  6 in total

1.  Detection of global hypermethylation in well-differentiated thyroid neoplasms by immunohistochemical (5-methylcytidine) analysis.

Authors:  S Keelawat; P S Thorner; S Shuangshoti; A Bychkov; N Kitkumthorn; P Rattanatanyong; W Boonyayothin; U Poumsuk; P Ruangvejvorachai; A Mutirangura
Journal:  J Endocrinol Invest       Date:  2015-03-05       Impact factor: 4.256

Review 2.  Emerging technologies for studying DNA methylation for the molecular diagnosis of cancer.

Authors:  Diego M Marzese; Dave Sb Hoon
Journal:  Expert Rev Mol Diagn       Date:  2015-03-22       Impact factor: 5.225

3.  Overexpression of CDKN2B (p15INK4B) and altered global DNA methylation status in mesenchymal stem cells of high-risk myelodysplastic syndromes.

Authors:  A Poloni; G Maurizi; D Mattiucci; S Amatori; B Fogliardi; B Costantini; M Mariani; S Mancini; A Olivieri; M Fanelli; P Leoni
Journal:  Leukemia       Date:  2014-06-19       Impact factor: 11.528

4.  Low Plasma Citrate Levels and Specific Transcriptional Signatures Associated with Quiescence of CD34+ Progenitors Predict Azacitidine Therapy Failure in MDS/AML Patients.

Authors:  Pavla Koralkova; Monika Belickova; David Kundrat; Michaela Dostalova Merkerova; Zdenek Krejcik; Katarina Szikszai; Monika Kaisrlikova; Jitka Vesela; Pavla Vyhlidalova; Jan Stetka; Alzbeta Hlavackova; Jiri Suttnar; Patrik Flodr; Jan Stritesky; Anna Jonasova; Jaroslav Cermak; Vladimir Divoky
Journal:  Cancers (Basel)       Date:  2021-04-30       Impact factor: 6.639

5.  Utility of 5-Methylcytosine Immunohistochemical Staining to Assess Global DNA Methylation and Its Prognostic Impact in MDS Patients

Authors:  Dinesh Chandra; Seema Tyagi; Jasdeep Singh; Roopam Deka; Prabhu Manivannan; Pravas Mishra; Hara Prasad Pati; Renu Saxena
Journal:  Asian Pac J Cancer Prev       Date:  2017-12-29

6.  Dysregulation and prognostic potential of 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), and 5-carboxylcytosine (5caC) levels in prostate cancer.

Authors:  Tine Maj Storebjerg; Siri H Strand; Søren Høyer; Anne-Sofie Lynnerup; Michael Borre; Torben F Ørntoft; Karina D Sørensen
Journal:  Clin Epigenetics       Date:  2018-08-07       Impact factor: 6.551

  6 in total

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