Clinical impact of LncRNA XIST and LncRNA NEAT1 for diagnosis of high-risk group breast cancer patients

Swellam, Menha; El Magdoub, Hekmat M; May Ahmed Shawki; Hefny, Mona M; El-Shazly, Samar Sami; Adel, M.;

Abstract


Long noncoding RNAs (lncRNAs) are evolving as contributing biomarkers for many diseases. Among these lncRNAs, X inactive-specific transcript (XIST), and nuclear paraspeckle assembly transcript 1 (NEAT1) were studied as undesirable upregulated nucleic acid markers for unfavorable prognosis of cancer. The authors aimed to investigate their role as diagnostic markers for breast cancer (BC) patients with high-risk factors. Serum samples were obtained from BC patients (n = 121), patients with benign breast lesions (n = 35), and healthy volunteers (n = 22). Assessment of lncRNA XIST, and lncRNA NEAT1 expression was performed using real time PCR. Expression levels of the investigated lncRNAs were significantly higher in BC patients as compared to the other groups. Both lncRNAs were significantly correlated with BC laterality, lymph node involvement, and clinical stages. LncRNA NEAT1 reported a significant aberrant expression with pathological types, histological grading and, hormonal status. The sensitivity of lncRNA NEAT1 was superior for detection of BC with high risk-factors as compared to lncRNA XIST. In conclusion, the detection of lncRNAs in body fluids has demonstrated a significant importance for detecting BC patients with high-risk factors, and was related to hormonal receptors, thus may be used for determining the direction of treatment strategy.


Other data

Title Clinical impact of LncRNA XIST and LncRNA NEAT1 for diagnosis of high-risk group breast cancer patients
Authors Swellam, Menha; El Magdoub, Hekmat M; May Ahmed Shawki ; Hefny, Mona M; El-Shazly, Samar Sami; Adel, M. 
Keywords Breast cancer diagnosis;Clinicopathological factors;NEAT1;Noninvasive;XIST;lncRNA
Issue Date Oct-2021
Publisher MOSBY-ELSEVIER
Journal Current problems in cancer 
Volume 45
Issue 5
ISSN 0147-0272
DOI 10.1016/j.currproblcancer.2021.100709
PubMed ID 33602501
Scopus ID 2-s2.0-85101390877
Web of science ID WOS:000727552100001

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