Evidence map›Paper›PMID 35954194›Full record

ReviewCells2022

Regulation of the Cancer Stem Phenotype by Long Non-Coding RNAs.

Jose Adan Gutierrez-Cruz, Vilma Maldonado, Jorge Melendez-Zajgla

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Jose Adan Gutierrez-CruzFunctional Genomics Laboratory, Instituto Nacional de Medicina Genomica, Mexico City 04710, Mexico.
Vilma MaldonadoEpigenetics Laboratory, Instituto Nacional de Medicina Genomica, Mexico City 04710, Mexico.
Jorge Melendez-ZajglaFunctional Genomics Laboratory, Instituto Nacional de Medicina Genomica, Mexico City 04710, Mexico.ORCID 0000-0002-2209-1607
National Institute of Genomic Medicine · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells are a cell population within malignant tumors that are characterized by the ability to self-renew, the presence of specific molecules that define their identity, the ability to form malignant tumors in vivo, resistance to drugs, and the ability to invade and migrate to other regions of the body. These characteristics are regulated by various molecules, such as lncRNAs, which are transcripts that generally do not code for proteins but regulate multiple biological processes through various mechanisms of action. LncRNAs, such as HOTAIR, H19, LncTCF7, LUCAT1, MALAT1, LINC00511, and FMR1-AS1, have been described as key regulators of stemness in cancer, allowing cancer cells to acquire this phenotype. It has been proposed that cancer stem cells are clinically responsible for the high recurrence rates after treatment and the high frequency of metastasis in malignant tumors, so understanding the mechanisms that regulate the stem phenotype could have an impact on the improvement of cancer treatments.

Indexed as

NeoplasmsRNA, Long NoncodingFragile X Messenger Ribonucleoprotein 1HumansNeoplastic Stem CellsPhenotypeFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1RNA, Long Noncodinglong non-coding RNAmicroenvironmentstem cancer cellsstem phenotype

Identifiers

PMID35954194
PMCPMC9367355
OpenAlexW4289109876

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.