Literature DB >> 26514535

Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/ Adult Acute Lymphoblastic Leukemia in Omani Patients.

Tadakal Mallana Goud1, Kamla Khalfan Al Salmani, Salma Mohammed Al Harasi, Muhanna Al Musalhi, Shah Mohammed Wasifuddin, Anna Rajab.   

Abstract

Genetic changes associated with acute lymphoblastic leukemia (ALL) provide very important diagnostic and prognostic information with a direct impact on patient management. Detection of chromosome abnormalities by conventional cytogenetics combined with fluorescence in situ hybridization (FISH) play a very significant role in assessing risk stratification. Identification of specific chromosome abnormalities has led to the recognition of genetic subgroups based on reciprocal translocations, deletions and modal number in B or T-cell ALL. In the last twelve years 102 newly diagnosed childhood/adult ALL bone marrow samples were analysed for chromosomal abnormalities with conventional G-banding, and FISH (selected cases) using specific probes in our hospital. G-banded karyotype analysis found clonal numerical and/or structural chromosomal aberrations in 74.2% of cases. Patients with pseudodiploidy represented the most frequent group (38.7%) followed by high hyperdiploidy group (12.9%), low hyperdiploidy group (9.7%), hypodiploidy (<46) group (9.7%) and high hypertriploidy group (3.2%). The highest observed numerical chromosomal alteration was high hyperdiploidy (12.9%) with abnormal karyotypes while abnormal 12p (7.5%) was the highest observed structural abnormality followed by t(12;21)(p13.3;q22) resulting in ETV6/RUNX1 fusion (5.4%) and t(9;22)(q34.1;q11.2) resulting in BCR/ABL1 fusion (4.3%). Interestingly, we identified 16 cases with rare and complex structural aberrations. Application of the FISH technique produced major improvements in the sensitivity and accuracy of cytogenetic analysis with ALL patients. In conclusion it confirmed heterogeneity of ALL by identifying various recurrent chromosomal aberrations along with non-specific rearrangements and their association with specific immunophenotypes. This study pool is representative of paediatric/adult ALL patients in Oman.

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Year:  2015        PMID: 26514535     DOI: 10.7314/apjcp.2015.16.16.7343

Source DB:  PubMed          Journal:  Asian Pac J Cancer Prev        ISSN: 1513-7368


  4 in total

1.  Cytogenetic Characteristics of Childhood Acute Lymphoblastic Leukemia: A Study of 1541 Chinese Patients Newly Diagnosed between 2001 and 2014.

Authors:  Meng-Meng Yin; Rui-Chi Wu; Jing Gao; Shao-Yan Hu; Xiao-Ming Liu; Xiao-Fan Zhu; Shu-Hong Shen; Jing-Yan Tang; Jing Chen; Qun Hu
Journal:  Curr Med Sci       Date:  2021-12-06

2.  Whole-Exome Sequencing of ETV6/RUNX1 in Four Childhood Acute Lymphoblastic Leukaemia Cases

Authors:  Zubaidah Zakaria; Norodiyah Othman; Azli Ismail; Nor Rizan Kamaluddin; Ezalia Esa; Eni Juraida Abdul Rahman; Yuslina Mat Yusoff; Fazlin Mohd Fauzi; Ten Sew Keoh
Journal:  Asian Pac J Cancer Prev       Date:  2017-04-01

3.  Identification of chromosomal abnormalities and genomic features in near-triploidy/tetraploidy-acute leukemia by fluorescence in situ hybridization.

Authors:  Ruqing Yang; Minghua Jiang; Junzhao Zhao; Hui Chen; Jian Gong; Yaying You; Laiyue Song; Zhen Li; Qian Li
Journal:  Cancer Manag Res       Date:  2019-02-15       Impact factor: 3.989

Review 4.  The spectrum of chromosomal translocations in the Arab world: ethnic-specific chromosomal translocations and their relevance to diseases.

Authors:  Hadeel T Zedan; Fatma H Ali; Hatem Zayed
Journal:  Chromosoma       Date:  2022-07-30       Impact factor: 2.919

  4 in total

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