Evidence map›Paper›PMID 33609219›Full record

ArticleMedical oncology (Northwood, London, England)2021

Elevated LINC01550 induces the apoptosis and cell cycle arrest of melanoma.

Jia Chen, Ping Li, Zizi Chen, Shaohua Wang, Shijie Tang, Xiang Chen, Zhizhao Chen, Jianda Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. MIMT1 and LINC01550 are uncharted lncRNAs down-regulated in colorectal cancer.International journal of experimental pathology · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. 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

8 authors at 2 institutions in 1 country.

Jia ChenDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital, Central South University, Changsha, 410013, China.
Ping LiDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital, Central South University, Changsha, 410013, China.
Zizi ChenDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital, Central South University, Changsha, 410013, China.
Shaohua WangDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital, Central South University, Changsha, 410013, China.
Shijie TangDepartment of Burns and Plastic Surgery, The Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, Guangdong, China.
Xiang ChenDepartment of Dermatology, XiangYa Hospital, Central South University, Changsha, 410008, China.
Zhizhao ChenDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital, Central South University, Changsha, 410013, China. czz657033698@126.com.
Jianda ZhouDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital, Central South University, Changsha, 410013, China. zhoujianda@csu.edu.cn.ORCID http://orcid.org/0000-0003-2760-2389
Central South University · CNShantou University · CN

Funding

the Scientific Research Fund Project of Hunan Provincial Health Commission B2015-040the Special Foundation of Basic Science and Technology Resources Survey of Ministry of Science and Technology of China 2017FY101204
6 · The paper itself

Abstract

Melanoma is a high-grade malignant subtype of human skin cancer with the highest mortality rate. Here we perform a bioinformatics analysis concerning human melanoma tissues by the Gene Expression Omnibus (GEO) database and Gene Expression Profiling Interactive Analysis (GEPIA) platform. We found that lncRNA LINC01550 was significantly down-regulated in the melanoma tissues as compared to the normal tissues. The low expression of LINC01550 was tightly associated with shorter overall survival and disease-free survival of patients with melanoma. LINC01550 expression is negatively associated with tumor cell proliferation and invasion abilities in melanoma as evidenced by the single-cell RNA sequencing (scRNA-seq) databases. LINC01550-overexpressing vectors were transferred into melanoma cells (WM35 and WM451). Up-regulation of LINC01550 significantly inhibited proliferation and invasion abilities, as well as induced cell apoptosis and G1 and S phase arrest of the melanoma cells. In conclusion, overexpression of LINC01550 may serve as a potential therapeutic target for melanoma.

Indexed as

ApoptosisCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationDown-RegulationGene ExpressionHumansMelanomaPrognosisRNA, Long NoncodingSkin NeoplasmsRNA, Long NoncodingApoptosisBioinformaticsCell cycleGEOLINC01550Melanoma

Identifiers

PMID33609219
OpenAlexW3129818825

What OpenQuestion holds

Textmetadata
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.