TY - JOUR
T1 - Population genetics of PDE4B (phosphodiesterase-4B) in neglected Native Americans
T2 - Implications for cancer pharmacogenetics
AU - Moreira, Rennan Garcias
AU - Saraiva-Duarte, Julia Maria
AU - Pereira, Alexandre Costa
AU - Sosa-Macias, Martha
AU - Galaviz-Hernandez, Carlos
AU - Santolalla, Meddly Lesley
AU - Magalhães, Wagner C.S.
AU - Zolini, Camila
AU - Leal, Thiago Peixoto
AU - Balázs, Zsolt
AU - Llerena, Adrián
AU - Gilman, Robert H.
AU - Mill, José Geraldo
AU - Borda, Victor
AU - Guio, Heinner
AU - O’Connor, Timothy D.
AU - Tarazona-Santos, Eduardo
AU - Rodrigues-Soares, Fernanda
N1 - Publisher Copyright:
© 2022 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.
PY - 2022/6
Y1 - 2022/6
N2 - PDE4B (phosphodiesterase-4B) has an important role in cancer and in pharmacology of some disorders, such as inflammatory diseases. Remarkably in Native Americans, PDE4B variants are associated with acute lymphoblastic leukemia (ALL) relapse, as this gene modulates sensitivity of glucocorticoids used in ALL chemotherapy. PDE4B allele rs6683977.G, associated with genomic regions of Native American origin in US-Hispanics (admixed among Native Americans, Europeans, and Africans), increases ALL relapse risk, contributing to an association between Native American ancestry and ALL relapse that disappeared with an extra-phase of chemotherapy. This result insinuates that indigenous populations along the Americas may have high frequencies of rs6683977.G, but this has never been corroborated. We studied ancestry and PDE4B diversity in 951 healthy individuals from nine Latin American populations. In non-admixed Native American populations rs6683977.G has frequencies greater than 90%, is in linkage disequilibrium with other ALL relapse associated and regulatory variants in PDE4B-intron-7, conforming haplotypes showing their highest worldwide frequencies in Native Americans (>0.82). Our findings inform the discussion on the pertinence of an extra-phase of chemotherapy in Native American populations, and exemplifies how knowledge generated in US-Hispanics is relevant for their even more neglected and vulnerable Native American ancestors along the American continent.
AB - PDE4B (phosphodiesterase-4B) has an important role in cancer and in pharmacology of some disorders, such as inflammatory diseases. Remarkably in Native Americans, PDE4B variants are associated with acute lymphoblastic leukemia (ALL) relapse, as this gene modulates sensitivity of glucocorticoids used in ALL chemotherapy. PDE4B allele rs6683977.G, associated with genomic regions of Native American origin in US-Hispanics (admixed among Native Americans, Europeans, and Africans), increases ALL relapse risk, contributing to an association between Native American ancestry and ALL relapse that disappeared with an extra-phase of chemotherapy. This result insinuates that indigenous populations along the Americas may have high frequencies of rs6683977.G, but this has never been corroborated. We studied ancestry and PDE4B diversity in 951 healthy individuals from nine Latin American populations. In non-admixed Native American populations rs6683977.G has frequencies greater than 90%, is in linkage disequilibrium with other ALL relapse associated and regulatory variants in PDE4B-intron-7, conforming haplotypes showing their highest worldwide frequencies in Native Americans (>0.82). Our findings inform the discussion on the pertinence of an extra-phase of chemotherapy in Native American populations, and exemplifies how knowledge generated in US-Hispanics is relevant for their even more neglected and vulnerable Native American ancestors along the American continent.
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U2 - 10.1111/cts.13266
DO - 10.1111/cts.13266
M3 - Article
C2 - 35266293
AN - SCOPUS:85127256971
SN - 1752-8054
VL - 15
SP - 1400
EP - 1405
JO - Clinical and Translational Science
JF - Clinical and Translational Science
IS - 6
ER -