Evidence map›Paper›PMID 31837057›Full record

ArticleJournal of clinical laboratory analysis2020

The implication of LncRNA MALAT1 in promoting chemo-resistance of laryngeal squamous cell carcinoma cells.

Qining Jiang, Shiying Liu, Linna Hou, Yanfei Guan, Shenggang Yang, Zhengyong Luo

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

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  13. tRNAJournal of clinical laboratory analysis · 2021
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  14. Tissue engineering of the larynx: A contemporary review.Journal of clinical laboratory analysis · 2021
    Review
  15. Review
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  18. Review
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

6 authors at 4 institutions in 1 country.

Qining JiangDepartment of Radiotherapy, Guizhou Cancer Hospital & The Affiliated Cancer Hospital of Guizhou Medical University, Guiyang, China.
Shiying LiuDepartment of Radiotherapy, Guizhou Cancer Hospital & The Affiliated Cancer Hospital of Guizhou Medical University, Guiyang, China.
Linna HouDepartment of Radiotherapy, Guizhou Cancer Hospital & The Affiliated Cancer Hospital of Guizhou Medical University, Guiyang, China.
Yanfei GuanDepartment of Otolaryngology-Head and Neck Surgery, The First People's Hospital of Yunnan Province, Kunming, China.
Shenggang YangDepartment of Radiotherapy, Yunnan Cancer Hospital & The Third Affiliated Hospital of Kunming Medical University, Kunming, China.ORCID https://orcid.org/0000-0001-5643-5212
Zhengyong LuoDepartment of Oncology, Puer People's Hospital, Puer, China.
Guiyang Medical University · CNFirst People's Hospital of Yunnan Province · CNKunming Medical University · CNPuer University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study was aimed to evaluate the involvement of lncRNA MALAT1 in modifying chemo-sensitivity of laryngeal squamous cell carcinoma (LSCC) cell lines.

methodsTotally 108 pairs of tumor tissues and matched para-tumor normal tissues were gathered from patients who were pathologically confirmed as LSCC. Meanwhile, LSCC cell lines, including TU686, TU177, AMC-HN-8, and LSC-1, were purchased to evaluate their tolerance to cisplatin, 5-fluorouracil, paclitaxel, and vincristine. Additionally, CCK-8 assay, flow cytometry, transwell assay, and wound healing assay were implemented to assess the part of MALAT1 in modulating viability, apoptosis, invasion, and migration of LSCC cell lines.

resultsMALAT1 expression was higher in LSCC tissues than in adjacent normal tissues (P < .05), and LSCC patients who carried highly expressed MALAT1 demonstrated poorer 5-year survival than ones with low MALAT1 expression (P < .05). For another, expression of MALAT1 was also unusually elevated within TU686, TU177, AMC-HN-8, and LSC-1 cell lines as relative to NHBEC cell line (P < .05). The TU686 cell line therein excelled in resisting the growth-curbing effects of 5-fluorouracil (IC50 = 20.44 μmol/L), paclitaxel (IC50 = 35.86 μg/L), and vincristine (IC50 = 0.12 μmol/L), when compared with TU177, AMC-HN-8, and LSC-1 cell line (P < .05). Moreover, there seemed great potential for over-expressed MALAT1 to enhance the chemo-resistance of both TU686 and LSC-1 cell lines (P < .05). Not only that, silencing of MALAT1 tended to undermine the proliferative and metastatic power of TU686 and LSC-1 cell lines (P < .05).

conclusionLncRNA MALAT1 counted in triggering tolerance of LSCC against chemo-drugs by boosting metastasis and depressing apoptosis of tumor cells.

Indexed as

ApoptosisCell Line, TumorCell MovementDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansLaryngeal NeoplasmsMaleMiddle AgedRNA, Long NoncodingSquamous Cell Carcinoma of Head and NeckMALAT1 long non-coding RNA, humanRNA, Long Noncodingchemo-sensitivityepithelial-mesenchymal transitionlaryngeal squamous cell carcinomaLncRNA MALAT1

Identifiers

PMID31837057
PMCPMC7171298
OpenAlexW2994721413

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.