Evidence map›Paper›PMID 32256118›Full record

ArticleCancer management and research2020

hsa_circRNA_101237: A Novel Diagnostic and Prognostic Biomarker and Potential Therapeutic Target for Multiple Myeloma.

Xiao Liu, Hao Tang, Jing Liu, Xiang Wang

Abstract read
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Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Review
  2. Circular RNAs and Cancers.Advances in experimental medicine and biology · 2025
    Review
  3. Article
  4. Review
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  6. Circular RNAs: typical biomarkers for bone-related diseases.Journal of Zhejiang University. Science. B · 2022
    Article
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  8. Review
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  16. Article
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  19. CircRNA ciRS-7: a Novel Oncogene in Multiple Cancers.International journal of biological sciences · 2021
    Review
  20. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiao Liu *The Third Xiangya Hospital of Central South University, Changsha 410013, People's Republic of China.
Hao Tang *The Third Xiangya Hospital of Central South University, Changsha 410013, People's Republic of China.
Jing LiuThe Third Xiangya Hospital of Central South University, Changsha 410013, People's Republic of China.
Xiang WangDepartment of Hematology, First Affiliated Hospital of Anhui Medical University, Hefei 230022, People's Republic of China.ORCID 0000-0001-9530-6157

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt has been demonstrated that circular RNA (circRNA) plays a crucial role in the occurrence and development of tumors, but the diagnostic and predictive value of most circRNAs in tumor patients remains unclear, especially for multiple myeloma (MM).

methodsHigh-throughput circRNA microarray-based sequencing was used to identify the differentially expressed circRNAs in MM. qRT-PCR was then employed to detect hsa_circRNA_101237 expression levels in the bone marrow tissues from 143 MM patients (65 first-episode treatment-naive patients and 78 patients with recurrent/refractory disease), MM cells and bortezomib-resistant MM cell lines. Whether hsa_circRNA_101237 can be used as a potential biomarker and therapeutic target for MM was investigated.

resultsThe average expressions of hsa_circRNA_101237 in the bone marrow tissues from MM patients (especially those with recurrent/refractory disease), MM cells and bortezomib-resistant MM cell lines were increased significantly (P<0.01). hsa_circRNA_101237 was overexpressed in patients positive for 13q14 deletion, 1q21 amplification, P53 deletion, and t(4,14) and t(14,16). hsa_circRNA_101237 was closely related to prognosis of the patients, and its high expression was associated with shorter OS and PFS. In addition, those overexpressing hsa_circRNA_101237 were less responsive to bortezomib treatment. Bioinformatic analysis indicated that hsa_circRNA_101237 interacted with 11 miRNAs and 10 candidate mRNAs. This finding may shed new light on the subsequent studies on the working mechanism and functions.

conclusionIt was first reported that hsa_circRNA_101237 was significantly upregulated in MM. It was indicated that hsa_circRNA_101237 may be a novel biomarker for MM, and it plays a significant role in the occurrence and development of MM.

Indexed as

biomarkercircRNAsdiagnosisMMprognosis

Identifiers

PMID32256118
PMCPMC7094164

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