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Comparative Profiling of Circulating Exosomal Small RNAs Derived From Peruvian Patients With Tuberculosis and Pulmonary Adenocarcinoma

  • Heinner Guio
  • , Victor Aliaga-Tobar
  • , Marco Galarza
  • , Oscar Pellon-Cardenas
  • , Silvia Capristano
  • , Henry L. Gomez
  • , Mivael Olivera
  • , Cesar Sanchez
  • , Vinicius Maracaja-Coutinho
  • Mental Honorio Delgado-Hideyo Noguchi
  • Universidad de Huánuco
  • Universidad de Chile
  • Rutgers University
  • Instituto Nacional de Enfermedades Neoplásicas Eduardo Cáceres Graziani
  • Instituto Vandique

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

14 Citas (Scopus)

Resumen

Tuberculosis (TB) is one of the most fatal infectious diseases, caused by the aerobic bacteria Mycobacterium tuberculosis. It is estimated that one-third of the world’s population is infected with the latent (LTB) version of this disease, with only 5-10% of infected individuals developing its active (ATB) form. Pulmonary adenocarcinoma (PA) is the most common and diverse form of primary lung carcinoma. The simultaneous or sequential occurrence of TB and lung cancer in patients has been widely reported and is known to be an issue for diagnosis and surgical treatment. Raising evidence shows that patients cured of TB represent a group at risk for developing PA. In this work, using sRNA-sequencing, we evaluated the expression patterns of circulating small RNAs available in exosomes extracted from blood samples of Peruvian patients affected by latent tuberculosis, active tuberculosis, or pulmonary adenocarcinoma. Differential expression analysis revealed a set of 24 microRNAs perturbed in these diseases, revealing potential biomarker candidates for the Peruvian population. Most of these miRNAs are normally expressed in healthy lung tissue and are potential regulators of different shared and unique KEGG pathways related to cancers, infectious diseases, and immunology.

Idioma originalInglés
Número de artículo909837
PublicaciónFrontiers in Cellular and Infection Microbiology
Volumen12
DOI
EstadoPublicada - 30 jun. 2022
Publicado de forma externa

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