Characterizing PML/RAR? Isoforms of Acute Promyelocytic Leukemia (APL) in Malay Patients

Authors

  • Rosline Hassan School of Medical Sciences, Universiti Sains Malaysia
  • Abu Dzarr Abdullah School of Medical Sciences, Universiti Sains Malaysia
  • Azlan Husin School of Medical Sciences, Universiti Sains Malaysia
  • Wan Zaidah Abdullah School of Medical Sciences, Universiti Sains Malaysia
  • Rapiaah Mustaffa School of Medical Sciences, Universiti Sains Malaysia
  • Selamah Ghazali School of Medical Sciences, Universiti Sains Malaysia
  • Cheng Yong ANG School of Medical Sciences, Universiti Sains Malaysia
  • Abdul Aziz Baba School of Medical Sciences, Universiti Sains Malaysia

DOI:

https://doi.org/10.3329/bjms.v13i3.15553

Keywords:

PML/RAR?, isoforms, APL, AML M3, nested RT-PCR

Abstract

Aim: Reciprocal translocation between retinoic acid receptor alpha (RAR?) gene on chromo- some 17 and promyelocytic leukemia (PML) gene on chromosome 15 is the hallmark for acute promyelocytic leukemia (APL). Three different PML/RAR? isoforms have been described; S-form, L-form and V-form. Our aims were to characterize the different types of PML/RAR? iso- forms in Malay patients with APL and to determine the outcome of these different types of iso-forms.

Materials and methods: RT-PCR analysis was performed on 20 patients recruited from hematology-oncology ward. RT-PCR detected fusion transcript of PML/RAR? in all patients.

Results and Discussion: Of these patients, 65% (13 patients) exhibited L/V-form, and 35% (7 patients) S-form. Total white blood cell count (TWBC) was higher in L/V-form (25 x 109/l) compared to S-form (2.1 x 109/l) (p < 0.05). Five years survival rate was 100% and 33.3% for L/V-forms and S-forms respectively (p<0.005).

Conclusion: We conclude that L/V- forms is the commonest isoform among Malays. They presented at younger age with higher TWBC counts. Although the sample size is small, our preliminary data showed an interestingly longer survival outcome among L/V-forms compared to S-form. PML/RAR? isoforms could be used in future as risk stratification feature in patients diagnosed as APL. Further study with more number of patients is required.

DOI: http://dx.doi.org/10.3329/bjms.v13i3.15553

Bangladesh Journal of Medical Science Vol.13(3) 2014 p.311-315

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Author Biographies

Rosline Hassan, School of Medical Sciences, Universiti Sains Malaysia

Department of Haematology

Abu Dzarr Abdullah, School of Medical Sciences, Universiti Sains Malaysia

Department of Medicine

Azlan Husin, School of Medical Sciences, Universiti Sains Malaysia

Department of Medicine

Wan Zaidah Abdullah, School of Medical Sciences, Universiti Sains Malaysia

Department of Haematology

Rapiaah Mustaffa, School of Medical Sciences, Universiti Sains Malaysia

Department of Haematology

Selamah Ghazali, School of Medical Sciences, Universiti Sains Malaysia

Department of Haematology

Cheng Yong ANG, School of Medical Sciences, Universiti Sains Malaysia

Department of Haematology

Abdul Aziz Baba, School of Medical Sciences, Universiti Sains Malaysia

Department of Medicine

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Published

2014-06-06

How to Cite

Hassan, R., Abdullah, A. D., Husin, A., Abdullah, W. Z., Mustaffa, R., Ghazali, S., ANG, C. Y., & Baba, A. A. (2014). Characterizing PML/RAR? Isoforms of Acute Promyelocytic Leukemia (APL) in Malay Patients. Bangladesh Journal of Medical Science, 13(3), 311–315. https://doi.org/10.3329/bjms.v13i3.15553

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Original Articles