Evidence map›Paper›PMID 37706018›Full record

ArticleHealth science reports2023

The expression of lncRNAs CASC2, NEAT1, LINC00299 in breast cancer tissues and their relationship with the XBP1 splicing rate in Iranian patients during 2014-2019: A cross-sectional study.

Ghazal Orak, Hossein Babaahmadi Rezaei, Fereshteh Ameli, Fatemeh Maghsoodi, Maryam Cheraghzade, Maryam Adelipour

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Article in Health science reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ghazal OrakDepartment of Clinical Biochemistry, School of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran.
Hossein Babaahmadi RezaeiDepartment of Clinical Biochemistry, School of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran.
Fereshteh AmeliDepartment of Pathology, School of Medicine Tehran University of Medical Science Tehran Iran.
Fatemeh MaghsoodiDepartment of Public Health Abadan University of Medical Sciences Abadan Iran.
Maryam CheraghzadeDepartment of Clinical Biochemistry, School of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran.
Maryam AdelipourDepartment of Clinical Biochemistry, School of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran.ORCID 0000-0002-5670-3595

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Breast cancer is a leading cause of incidence and mortality in women globally. Identifying new molecular markers can aid in cancer diagnosis, targeted therapy, and treatment monitoring. This study aimed to measure the expression of the X-box binding protein 1 (XBP1) gene, an index of the unfolded protein response (UPR), and long noncoding RNAs (lncRNAs), including Nuclear Enriched Abundant Transcript 1 (NEAT1), Cancer Susceptibility Candidate 2 (CASC2), and Long Intergenic Nonprotein Coding RNA 299 (LINC00299), as possible regulators of the UPR pathway. Methods: Total RNA was extracted from 40 samples of breast tumor tissues and their respective controls. The expression level of lncRNAs CASC2, NEAT1, and LINC00299 was quantified using reverse transcription-polymerase chain reaction (RT-PCR). The ratio of the spliced form of XBP1 to its unspliced form (XBP1u) was determined by PCR and electrophoresis. Results: The results showed a 2.8-fold increase in the ratio of XBP1s/u in breast cancer tissues compared to adjacent nonmalignant samples ( Conclusions: Based on the association between the expression of lncRNAs CASC2, LINC00299, and NEAT1 and the XBP1s/u ratio, these lncRNAs could be potential regulators of the UPR pathway. Also, CASC2 and NEAT1 genes could be suggested as suitable biomarkers to distinguish cancerous tissue from noncancerous breast tissue due to their significant increase in expression in cancerous samples compared to adjacent noncancerous.

Indexed as

breast neoplasmsgene expressionlong noncoding RNAXBP1

Identifiers

PMID37706018
PMCPMC10495808

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.