Subtipos moleculares de PML/RARα en pacientes con leucemia promielocítica aguda
Bibliographic Data
| ID | 15533883 |
|---|---|
| Authors | María del Carmen Castro‐Mujica (0000-0003-4404-2133, Instituto Nacional de Enfermedades Neoplásicas, corresponding author), María del Carmen Castro-Mujica, Yasser Sullcahuamán-Allende (Instituto Nacional de Enfermedades Neoplásicas) |
| Year | 2013 |
| Volume | 30 |
| Issue | 1 |
| Pages | 37-40 |
| Publication date | 2013-03-01 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Revista Peruana de Medicina Experimental y Salud Pública (JOURNAL) |
| Journal identifiers | ISSN: 1726-4634 • E-ISSN: 1726-4642 |
| Publisher | National Institute of Health of Peru (PUBLISHER • PE) |
| DOI | 10.1590/s1726-46342013000100007 |
| PMID | 23612809 |
| OpenAlex | W1996255186 |
| SciELO | S1726-46342013000100007 |
| Language | ES |
The objective was to describe the frequency of molecular subtypes of PML/RARα in patients with acute promyelocytic leukemia (APL) and their distribution according to risk of recurrence and cytomorphology. A case series was carried out, including fifty patients registered at the National Institute of Neoplastic Diseases (INEN) during 2010-2012, with molecular diagnosis of APL PML/RARα and bcr1, bcr2 and bcr3 subtypes by reverse-transcription polymerase chain reaction (RT-PCR). Bcr1 subtype was the most frequent (62%). Most patients with an intermediate risk of recurrence and hypergranular morphology were bcr1 (70%), while all patients with high risk of recurrence and hypogranular morphology were bcr3. A predominance of bcr1 subtype among the population studied can therefore be concluded, as well as the fact that there are differences in the distribution of bcr1 and bcr3 subtypes according to recurrence risk group and cytomorphology
Acute promyelocytic leukemia · Biology · Gene · Gene expression · Pathology · Population · Reverse transcription polymerase chain reaction · Acute Lymphoblastic Leukemia research · Acute Myeloid Leukemia Research · Medicine · Retinoids in leukemia and cellular processes · Gastroenterology · Genetics · Internal Medicine · Oncology
| Highly cited | No |
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