Circulating miRNA‐375 as a potential novel biomarker for active Kaposi’s sarcoma in AIDS patients

The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by AIDS‐Kaposi's sarcoma (KS). Screening of 377 miRNAs was performed using low‐density arrays in pooled plasma samples of 10 HIV/human herpesvirus 8 (HHV8)‐i...

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Published inJournal of cellular and molecular medicine Vol. 23; no. 2; pp. 1486 - 1494
Main Authors Piano, Maria Assunta, Gianesello, Lisa, Grassi, Angela, Del Bianco, Paola, Mattiolo, Adriana, Cattelan, Anna Maria, Sasset, Lolita, Zanovello, Paola, Calabrò, Maria Luisa
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Published England John Wiley & Sons, Inc 01.02.2019
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Abstract The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by AIDS‐Kaposi's sarcoma (KS). Screening of 377 miRNAs was performed using low‐density arrays in pooled plasma samples of 10 HIV/human herpesvirus 8 (HHV8)‐infected asymptomatic and 10 AIDS‐KS patients before and after successful combined antiretroviral therapy (cART). MiR‐375 was identified as a potential marker of active KS, being the most down‐regulated in AIDS‐KS patients after cART and the most up‐regulated in naïve AIDS‐KS patients compared to naïve asymptomatic subjects. Validation on individual plasma samples confirmed that miR‐375 levels were higher in AIDS‐KS compared to asymptomatic patients, decreased after cART‐induced remission in most AIDS‐KS patients and increased in patients with active KS. In asymptomatic patients miR‐375 was up‐regulated after cART in both screening and validation. Statistical analyses revealed an association between miR‐375 changes and CD4 cell counts, which could explain the discordant cases and the opposite trend between asymptomatic and AIDS‐KS patients. These data suggest that circulating miR‐375 might be a good indicator of active AIDS‐KS. Moreover, changes in miR‐375 levels may have a prognostic value in HIV/HHV8‐infected patients undergoing treatment. Further large‐scale validation is needed.
AbstractList Abstract The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by AIDS‐Kaposi's sarcoma (KS). Screening of 377 miRNAs was performed using low‐density arrays in pooled plasma samples of 10 HIV/human herpesvirus 8 (HHV8)‐infected asymptomatic and 10 AIDS‐KS patients before and after successful combined antiretroviral therapy (cART). MiR‐375 was identified as a potential marker of active KS, being the most down‐regulated in AIDS‐KS patients after cART and the most up‐regulated in naïve AIDS‐KS patients compared to naïve asymptomatic subjects. Validation on individual plasma samples confirmed that miR‐375 levels were higher in AIDS‐KS compared to asymptomatic patients, decreased after cART‐induced remission in most AIDS‐KS patients and increased in patients with active KS. In asymptomatic patients miR‐375 was up‐regulated after cART in both screening and validation. Statistical analyses revealed an association between miR‐375 changes and CD4 cell counts, which could explain the discordant cases and the opposite trend between asymptomatic and AIDS‐KS patients. These data suggest that circulating miR‐375 might be a good indicator of active AIDS‐KS. Moreover, changes in miR‐375 levels may have a prognostic value in HIV/HHV8‐infected patients undergoing treatment. Further large‐scale validation is needed.
The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by AIDS‐Kaposi's sarcoma (KS). Screening of 377 miRNAs was performed using low‐density arrays in pooled plasma samples of 10 HIV/human herpesvirus 8 (HHV8)‐infected asymptomatic and 10 AIDS‐KS patients before and after successful combined antiretroviral therapy (cART). MiR‐375 was identified as a potential marker of active KS, being the most down‐regulated in AIDS‐KS patients after cART and the most up‐regulated in naïve AIDS‐KS patients compared to naïve asymptomatic subjects. Validation on individual plasma samples confirmed that miR‐375 levels were higher in AIDS‐KS compared to asymptomatic patients, decreased after cART‐induced remission in most AIDS‐KS patients and increased in patients with active KS. In asymptomatic patients miR‐375 was up‐regulated after cART in both screening and validation. Statistical analyses revealed an association between miR‐375 changes and CD4 cell counts, which could explain the discordant cases and the opposite trend between asymptomatic and AIDS‐KS patients. These data suggest that circulating miR‐375 might be a good indicator of active AIDS‐KS. Moreover, changes in miR‐375 levels may have a prognostic value in HIV/HHV8‐infected patients undergoing treatment. Further large‐scale validation is needed.
Author Calabrò, Maria Luisa
Mattiolo, Adriana
Sasset, Lolita
Zanovello, Paola
Gianesello, Lisa
Del Bianco, Paola
Piano, Maria Assunta
Grassi, Angela
Cattelan, Anna Maria
AuthorAffiliation 2 Clinical Trials and Biostatistics Veneto Institute of Oncology IOV ‐ IRCCS Padova Italy
1 Immunology and Molecular Oncology Veneto Institute of Oncology IOV ‐ IRCCS Padova Italy
3 Infectious and Tropical Diseases Azienda Ospedaliera and University of Padova Padova Italy
5 Department of Surgery, Oncology and Gastroenterology University of Padova Padova Italy
6 Present address: Clinical Nephrology, Department of Medicine University of Padova Padova Italy
4 Infectious Diseases ULSS 18 ‐ Azienda Ospedaliera Rovigo Italy
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– name: 6 Present address: Clinical Nephrology, Department of Medicine University of Padova Padova Italy
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Copyright 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
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Issue 2
Keywords HHV8
HIV
Kaposi’s sarcoma
miR-375
circulating miRNA
microRNA
biomarker
Language English
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2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
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Notes This work was supported by Associazione Italiana per la Ricerca sul Cancro and Fondazione Cariverona (grant no. 6599) and by 5X1000‐IOV2010 (grant CUP no. J94G13000140001 to MLC). MAP, LG, and AM were recipients of a Ricerca Corrente fellowship, Italian Ministry of Health (IMH). IMH funding was also used for payment of the publication fee.
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Maria Assunta Piano, Lisa Gianesello and Angela Grassi contributed equally to this study.
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Snippet The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by AIDS‐Kaposi's...
The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by AIDS-Kaposi's...
Abstract The aim of this study was to identify circulating microRNAs (miRNAs) that could be used as biomarkers in patients at risk for or affected by...
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SubjectTerms Acquired immune deficiency syndrome
Acquired Immunodeficiency Syndrome - blood
Acquired Immunodeficiency Syndrome - pathology
Acquired Immunodeficiency Syndrome - virology
Adult
AIDS
Antiretroviral agents
Antiretroviral therapy
Antiretroviral Therapy, Highly Active
Bioindicators
biomarker
Biomarkers
Biomarkers, Tumor - blood
CD4 antigen
Circulating MicroRNA - blood
circulating miRNA
Female
Herpesvirus 8, Human - pathogenicity
HHV8
HIV
HIV Infections - blood
HIV Infections - pathology
HIV Infections - virology
Human immunodeficiency virus
Humans
Kaposi's sarcoma
Kaposis sarcoma
Male
microRNA
MicroRNAs - blood
Middle Aged
miRNA
miR‐375
Original
Patients
Remission
Sarcoma
Sarcoma, Kaposi - blood
Sarcoma, Kaposi - pathology
Sarcoma, Kaposi - virology
Statistical analysis
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Title Circulating miRNA‐375 as a potential novel biomarker for active Kaposi’s sarcoma in AIDS patients
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjcmm.14054
https://www.ncbi.nlm.nih.gov/pubmed/30549196
https://www.proquest.com/docview/2171685998
https://search.proquest.com/docview/2157645250
https://pubmed.ncbi.nlm.nih.gov/PMC6349189
Volume 23
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