Author/Authors :
Sheikhpour, Mojgan Department of Mycobacteriology and Pulmonary Research - Pasteur Institute of Iran, Tehran, Iran , Abolfathi, Hanie Department of Mycobacteriology and Pulmonary Research - Pasteur Institute of Iran, Tehran, Iran , Karimipoor, Morteza Department of Molecular Medicine - Biotechnology Research Center - Pasteur Institute of Iran, Tehran, Iran , Movafagh, Abolfazl Department of Medical Genetics - Cancer Research Center, Shohada Hospital - School of Medicine - Shahid Beheshti University of Medical Science, Tehran, Iran , Shahsavani, Mahbubeh Department of Genetics & Biotechnology - School of Biological Science - Pishva Branch, Islamic Azad University, Varamin, Iran
Abstract :
Tuberculosis (TB) and non-small cell lung cancer (NSCLC) are two major
contributors to mortality and morbidity worldwide. In this regard, TB and
NSCLC have similar symptoms, and TB has symptoms that are identical to
malignancy; therefore, sometimes it is mistakenly diagnosed as lung cancer.
Moreover, patients with active pulmonary TB are at a higher risk of dying due
to lung cancer. In addition, several signaling pathways involved in TB and
NSCLC have been identified. Also, the miRNAs are biological molecules shown
to play essential roles in the above-mentioned diseases through targeting the
signaling pathways’ genes. Most of the pathways affected by miRNAs are
immune responses such as autophagy and apoptosis in TB and NSCLC,
respectively. Several studies have separately investigated the expression of
miRNAs profile in patients with NSCLC and infectious TB. In this critical
review, we attempted to gather common miRNAs between TB and NSCLC and
to explain the involved-pathways, which are affected by miRNAs in both TB
and NSCLC. Results of this critical review show that the expressions of miR-
155, miR-146a, miR-125b, miR-30a, miR-29a, and miR-Let7 have significantly
changed in TB and NSCLC. The data suggest that miRNAs expression may
provide a new method for screening or differential diagnosis of NSCLC and TB.
Keywords :
Tuberculosis , Non-small cell lung cancer , miRNA , Expression