2014, Number 3
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Rev Hosp Jua Mex 2014; 81 (3)
Citogenómica en leucemia linfoblástica aguda
Bravata-Alcántara JC, Chávez-Ocaña S, Sierra-Martínez M
Language: Spanish
References: 17
Page: 182-187
PDF size: 292.83 Kb.
ABSTRACT
In acute lymphoblastic leukemia (ALL), various types of chromosomal alterations with prognostic value are reported
well known, these changes allow us to evaluate the response to treatment and survival. Cytogenomics currently
allows to know the behavior of leukemias using high-density microarrays, as it has been observed that higher
detection. With microarrays can detect losses that are closely related genes as clinically;
CDKN2A/B, ETV6, PAX5
and
IKZF1, which are associated with the expression and regulation of genes that contribute to neoplastic
transformation in hematopoiesis and are located in cells of type B. With these technological advances in microarray
platforms, we have allowed more knowledge to understand the processes of leukemogenesis, for therapeutic
targets, and deliver personalized medicine. But we still need to understand mechanisms that allow us to identify
why there are differences in the origin and frequency of chromosome abnormalities among children and adults.
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