Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project

One recently identified subtype of pediatric B-precursor acute lymphoblastic leukemia (ALL) has been termed BCR-ABL1-like or Ph-like because of similarity of the gene expression profile to BCR-ABL1 positive ALL suggesting the presence of lesions activating tyrosine kinases, frequent alteration of IK...

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Vydané v:Blood Ročník 121; číslo 3; s. 485
Hlavní autori: Loh, Mignon L, Zhang, Jinghui, Harvey, Richard C, Roberts, Kathryn, Payne-Turner, Debbie, Kang, Huining, Wu, Gang, Chen, Xiang, Becksfort, Jared, Edmonson, Michael, Buetow, Kenneth H, Carroll, William L, Chen, I-Ming, Wood, Brent, Borowitz, Michael J, Devidas, Meenakshi, Gerhard, Daniela S, Bowman, Paul, Larsen, Eric, Winick, Naomi, Raetz, Elizabeth, Smith, Malcolm, Downing, James R, Willman, Cheryl L, Mullighan, Charles G, Hunger, Stephen P
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 17.01.2013
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Abstract One recently identified subtype of pediatric B-precursor acute lymphoblastic leukemia (ALL) has been termed BCR-ABL1-like or Ph-like because of similarity of the gene expression profile to BCR-ABL1 positive ALL suggesting the presence of lesions activating tyrosine kinases, frequent alteration of IKZF1, and poor outcome. Prior studies demonstrated that approximately half of these patients had genomic lesions leading to CRLF2 overexpression, with half of such cases harboring somatic mutations in the Janus kinases JAK1 and JAK2. To determine whether mutations in other tyrosine kinases might also occur in ALL, we sequenced the tyrosine kinome and downstream signaling genes in 45 high-risk pediatric ALL cases with either a Ph-like gene expression profile or other alterations suggestive of activated kinase signaling. Aside from JAK mutations and 1 FLT3 mutation, no somatic mutations were found in any other tyrosine kinases, suggesting that alternative mechanisms are responsible for activated kinase signaling in high-risk ALL.
AbstractList One recently identified subtype of pediatric B-precursor acute lymphoblastic leukemia (ALL) has been termed BCR-ABL1-like or Ph-like because of similarity of the gene expression profile to BCR-ABL1 positive ALL suggesting the presence of lesions activating tyrosine kinases, frequent alteration of IKZF1, and poor outcome. Prior studies demonstrated that approximately half of these patients had genomic lesions leading to CRLF2 overexpression, with half of such cases harboring somatic mutations in the Janus kinases JAK1 and JAK2. To determine whether mutations in other tyrosine kinases might also occur in ALL, we sequenced the tyrosine kinome and downstream signaling genes in 45 high-risk pediatric ALL cases with either a Ph-like gene expression profile or other alterations suggestive of activated kinase signaling. Aside from JAK mutations and 1 FLT3 mutation, no somatic mutations were found in any other tyrosine kinases, suggesting that alternative mechanisms are responsible for activated kinase signaling in high-risk ALL.
One recently identified subtype of pediatric B-precursor acute lymphoblastic leukemia (ALL) has been termed BCR-ABL1-like or Ph-like because of similarity of the gene expression profile to BCR-ABL1 positive ALL suggesting the presence of lesions activating tyrosine kinases, frequent alteration of IKZF1, and poor outcome. Prior studies demonstrated that approximately half of these patients had genomic lesions leading to CRLF2 overexpression, with half of such cases harboring somatic mutations in the Janus kinases JAK1 and JAK2. To determine whether mutations in other tyrosine kinases might also occur in ALL, we sequenced the tyrosine kinome and downstream signaling genes in 45 high-risk pediatric ALL cases with either a Ph-like gene expression profile or other alterations suggestive of activated kinase signaling. Aside from JAK mutations and 1 FLT3 mutation, no somatic mutations were found in any other tyrosine kinases, suggesting that alternative mechanisms are responsible for activated kinase signaling in high-risk ALL.One recently identified subtype of pediatric B-precursor acute lymphoblastic leukemia (ALL) has been termed BCR-ABL1-like or Ph-like because of similarity of the gene expression profile to BCR-ABL1 positive ALL suggesting the presence of lesions activating tyrosine kinases, frequent alteration of IKZF1, and poor outcome. Prior studies demonstrated that approximately half of these patients had genomic lesions leading to CRLF2 overexpression, with half of such cases harboring somatic mutations in the Janus kinases JAK1 and JAK2. To determine whether mutations in other tyrosine kinases might also occur in ALL, we sequenced the tyrosine kinome and downstream signaling genes in 45 high-risk pediatric ALL cases with either a Ph-like gene expression profile or other alterations suggestive of activated kinase signaling. Aside from JAK mutations and 1 FLT3 mutation, no somatic mutations were found in any other tyrosine kinases, suggesting that alternative mechanisms are responsible for activated kinase signaling in high-risk ALL.
Author Kang, Huining
Devidas, Meenakshi
Raetz, Elizabeth
Willman, Cheryl L
Edmonson, Michael
Larsen, Eric
Zhang, Jinghui
Becksfort, Jared
Wu, Gang
Roberts, Kathryn
Carroll, William L
Harvey, Richard C
Downing, James R
Payne-Turner, Debbie
Chen, I-Ming
Winick, Naomi
Wood, Brent
Chen, Xiang
Gerhard, Daniela S
Bowman, Paul
Loh, Mignon L
Buetow, Kenneth H
Hunger, Stephen P
Smith, Malcolm
Borowitz, Michael J
Mullighan, Charles G
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Snippet One recently identified subtype of pediatric B-precursor acute lymphoblastic leukemia (ALL) has been termed BCR-ABL1-like or Ph-like because of similarity of...
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StartPage 485
SubjectTerms Child
Child, Preschool
Disease-Free Survival
Female
fms-Like Tyrosine Kinase 3 - genetics
fms-Like Tyrosine Kinase 3 - metabolism
Gene Expression Regulation, Leukemic - physiology
Humans
Infant
Janus Kinase 1 - genetics
Janus Kinase 1 - metabolism
Janus Kinase 2 - genetics
Janus Kinase 2 - metabolism
Male
Neoplasm, Residual - enzymology
Neoplasm, Residual - genetics
Neoplasm, Residual - mortality
Philadelphia Chromosome
Precursor Cell Lymphoblastic Leukemia-Lymphoma - enzymology
Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality
Protein-Tyrosine Kinases - genetics
Protein-Tyrosine Kinases - metabolism
Receptors, Cytokine - genetics
Receptors, Cytokine - metabolism
Receptors, Purinergic P2Y - genetics
Receptors, Purinergic P2Y - metabolism
Signal Transduction - genetics
Transcriptome
Title Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project
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