Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma

Anaplastic large cell lymphomas associated with ALK translocation have a good outcome after CHOP treatment; however, the 2-year relapse rate remains at 30%. Microarray gene-expression profiling of 48 samples obtained at diagnosis was used to identify 47 genes that were differentially expressed betwe...

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Autores principales: Daugrois Camille, Bessiere Chloé, Dejean Sébastien, Anton Leberre Véronique, Commes Thérèse, Stephane Pyronnet, Pierre Brousset, Estelle Espinos, Brugiere Laurence, Fabienne Meggetto, Laurence Lamant
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/664c157e324b4ccaac7c1d17057220bf
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spelling oai:doaj.org-article:664c157e324b4ccaac7c1d17057220bf2021-11-11T15:33:52ZGene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma10.3390/cancers132155232072-6694https://doaj.org/article/664c157e324b4ccaac7c1d17057220bf2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/21/5523https://doaj.org/toc/2072-6694Anaplastic large cell lymphomas associated with ALK translocation have a good outcome after CHOP treatment; however, the 2-year relapse rate remains at 30%. Microarray gene-expression profiling of 48 samples obtained at diagnosis was used to identify 47 genes that were differentially expressed between patients with early relapse/progression and no relapse. In the relapsing group, the most significant overrepresented genes were related to the regulation of the immune response and T-cell activation while those in the non-relapsing group were involved in the extracellular matrix. Fluidigm technology gave concordant results for 29 genes, of which FN1, FAM179A, and SLC40A1 had the strongest predictive power after logistic regression and two classification algorithms. In parallel with 39 samples, we used a Kallisto/Sleuth pipeline to analyze RNA sequencing data and identified 20 genes common to the 28 genes validated by Fluidigm technology—notably, the <i>FAM179A</i> and <i>FN1</i> genes. Interestingly, FN1 also belongs to the gene signature predicting longer survival in diffuse large B-cell lymphomas treated with CHOP. Thus, our molecular signatures indicate that the FN1 gene, a matrix key regulator, might also be involved in the prognosis and the therapeutic response in anaplastic lymphomas.Daugrois CamilleBessiere ChloéDejean SébastienAnton Leberre VéroniqueCommes ThérèseStephane PyronnetPierre BroussetEstelle EspinosBrugiere LaurenceFabienne MeggettoLaurence LamantMDPI AGarticleALK<sup>+</sup> ALCLpredictive signaturerelapseclinical outcomeNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5523, p 5523 (2021)
institution DOAJ
collection DOAJ
language EN
topic ALK<sup>+</sup> ALCL
predictive signature
relapse
clinical outcome
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle ALK<sup>+</sup> ALCL
predictive signature
relapse
clinical outcome
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Daugrois Camille
Bessiere Chloé
Dejean Sébastien
Anton Leberre Véronique
Commes Thérèse
Stephane Pyronnet
Pierre Brousset
Estelle Espinos
Brugiere Laurence
Fabienne Meggetto
Laurence Lamant
Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma
description Anaplastic large cell lymphomas associated with ALK translocation have a good outcome after CHOP treatment; however, the 2-year relapse rate remains at 30%. Microarray gene-expression profiling of 48 samples obtained at diagnosis was used to identify 47 genes that were differentially expressed between patients with early relapse/progression and no relapse. In the relapsing group, the most significant overrepresented genes were related to the regulation of the immune response and T-cell activation while those in the non-relapsing group were involved in the extracellular matrix. Fluidigm technology gave concordant results for 29 genes, of which FN1, FAM179A, and SLC40A1 had the strongest predictive power after logistic regression and two classification algorithms. In parallel with 39 samples, we used a Kallisto/Sleuth pipeline to analyze RNA sequencing data and identified 20 genes common to the 28 genes validated by Fluidigm technology—notably, the <i>FAM179A</i> and <i>FN1</i> genes. Interestingly, FN1 also belongs to the gene signature predicting longer survival in diffuse large B-cell lymphomas treated with CHOP. Thus, our molecular signatures indicate that the FN1 gene, a matrix key regulator, might also be involved in the prognosis and the therapeutic response in anaplastic lymphomas.
format article
author Daugrois Camille
Bessiere Chloé
Dejean Sébastien
Anton Leberre Véronique
Commes Thérèse
Stephane Pyronnet
Pierre Brousset
Estelle Espinos
Brugiere Laurence
Fabienne Meggetto
Laurence Lamant
author_facet Daugrois Camille
Bessiere Chloé
Dejean Sébastien
Anton Leberre Véronique
Commes Thérèse
Stephane Pyronnet
Pierre Brousset
Estelle Espinos
Brugiere Laurence
Fabienne Meggetto
Laurence Lamant
author_sort Daugrois Camille
title Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma
title_short Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma
title_full Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma
title_fullStr Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma
title_full_unstemmed Gene Expression Signature Associated with Clinical Outcome in ALK-Positive Anaplastic Large Cell Lymphoma
title_sort gene expression signature associated with clinical outcome in alk-positive anaplastic large cell lymphoma
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/664c157e324b4ccaac7c1d17057220bf
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