Evidence map›Paper›PMID 34508305›Full record

ReviewHuman cell2021

Research progress of DLX6-AS1 in human cancers.

Yalan Luo, Peng Ge, Mengfei Wang, Haiyang Chen, Jiayue Liu, Tianfu Wei, Yuankuan Jiang, Jialin Qu, Hailong Chen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Human cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

9 authors at 1 institution in 1 country.

Yalan Luo *Department of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China.
Peng Ge *Department of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China.
Mengfei Wang *Department of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China.
Haiyang ChenDepartment of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China.
Jiayue LiuDepartment of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China.
Tianfu WeiDepartment of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China.
Yuankuan JiangInstitute (College) of Integrative Medicine, Dalian Medical University, Dalian, 116044, People's Republic of China.
Jialin QuInstitute (College) of Integrative Medicine, Dalian Medical University, Dalian, 116044, People's Republic of China. jialin_qu@126.com.
Hailong ChenDepartment of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, People's Republic of China. chenhailong@dmu.edu.cn.ORCID http://orcid.org/0000-0001-5247-7343
Dalian Medical University · CN

Funding

National Natural Science Foundation of China 82074158
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) are a kind of translational-repressor RNAs composed of more than 200 nucleotides and formerly considered as "transcriptional noise". Recently studies have shown that lncRNAs could bind to multiple biomolecules such as DNA, transcription factors, RNA, chromatin complexes and proteins, and regulate target gene expression at multi-levels, thus playing an essential role in human tumors. DLX6-AS1, a recently discovered oncogenic lncRNA, is highly expressed in various human tumors, including lung cancer, liver cancer and pancreatic cancer. This paper mainly reviewed the regulatory mechanism of DLX6-AS1 as a competitive endogenous RNA (ceRNA) in tumor cell proliferation, cell apoptosis, angiogenesis, epithelial-mesenchymal transformation, chemotherapy resistance and metabolic changes. Furthermore, the translational value of DLX6-AS1 in cancer was also elucidated, which suggested its potential as a diagnostic or prognostic biomarker in cancer. In summary, this present article not only makes an in-depth analysis of the expression changes and carcinogenic mechanism of DLX6-AS1 in various human cancers, but also provides a new breakthrough for the diagnosis and treatment of cancers.

Indexed as

Biomarkers, TumorApoptosisCell ProliferationDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionGene ExpressionGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansMolecular Targeted TherapyNeoplasmsNeovascularization, PathologicPrognosisProtein BiosynthesisBiomarkers, TumorDLX6 protein, humanHomeodomain ProteinsBiomarkerDLX6-AS1LncRNATherapeuticTumors

Identifiers

PMID34508305
OpenAlexW3197769284

What Socratic 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 Socratic graph.