Evidence map›Paper›PMID 34094941›Full record

ArticleFrontiers in oncology2021

lncRNA MIAT/HMGB1 Axis Is Involved in Cisplatin Resistance

Xuewei Zhu, Li Liu, Yang Wang, Jianan Cong, Zhang Lin, Yongsen Wang, Qi Liu, Leiming Wang, Ben Yang, Tao Li

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Unraveling the complexity of STAT3 in cancer: molecular understanding and drug discovery.Journal of experimental & clinical cancer research : CR · 2024
    Review
  4. Multiple functions of HMGB1 in cancer.Frontiers in oncology · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Xuewei ZhuDepartment of Otolaryngology Head & Neck Surgery, China Japan Union Hospital of Jilin University, Changchun, China.
Li LiuReproductive Medical Center, Department of Gynecology and Obstetrics, China-Japan Union Hospital of Jilin University, Changchun, China.
Yang WangDepartment of Dermatology, The Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, China.
Jianan CongDepartment of Ophthalmology, Changchun City Central Hospital, Changchun, China.
Zhang LinDepartment of Ophthalmology, China-Japan Union Hospital, Jilin University, Changchun, China.
Yongsen WangTechnology Department, Harbin Boshixuan Technology Co., Ltd, Harbin, China.
Qi LiuDepartment of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
Leiming WangShenzhen Bay Laboratory, The Institute of Chemical Biology, Gaoke International Innovation Center, Shenzhen, China.
Ben YangDepartment of Ophthalmology, China-Japan Union Hospital, Jilin University, Changchun, China.
Tao LiDepartment of Anesthesiology, China-Japan Union Hospital of Jilin University, Changchun, China.
Union Hospital · CNChangchun University of Chinese Medicine · CNJilin University · CNChangchun Obstetrics and Gynecology Hospital · CNShenzhen Bay Laboratory · CNThe University of Texas Health Science Center at San Antonio · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cisplatin-based chemotherapy and radiotherapy are the main first-line treatment strategies for nasopharyngeal carcinoma (NPC) patients. Unfortunately, resistance is a major obstacle in the clinical management of NPC patients. We prove that the expression level of high-mobility group box 1 (HMGB1) is dramatically increased in resistant NPC cells than that in sensitive cells. HMGB1 induces the expression and secretion of IL6, which leads to constitutive autocrine activation of the JAK2/STAT3 pathway and eventually contributes to chemoresistance in NPC cells. Long non-coding RNAs (lncRNAs) have been identified as key regulators involved in drug resistance. In this study, using GO analysis of the biological process and differential expression analysis, we find 12 significantly altered IncRNAs in NPC cell lines, which may be involved in regulating gene expression. Furthermore, we determine that elevated lncRNA MIAT level upregulates HMGB1 expression, contributing to cisplatin resistance in NPC cells. We find that the deficiency of the lncRNA MIAT/HMGB1 axis, inhibition of JAK2/STAT3, or neutralization of IL6 by antibodies significantly re-sensitizes resistant NPC cells to cisplatin in resistant NPC cells. Moreover, we provide the

Indexed as

cisplatin resistanceHMGB1IL6lncRNA MIATNPC

Identifiers

PMID34094941
PMCPMC8173225
OpenAlexW3165486194

What OpenQuestion holds

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Registered trials

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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.