Evidence map›Paper›PMID 30712429›Full record

ArticleCell cycle (Georgetown, Tex.)2019

Chromatin accessibility changes are associated with enhanced growth and liver metastasis capacity of acid-adapted colorectal cancer cells.

Zhi-Hang Zhou, Qing-Liang Wang, Lin-Hong Mao, Xiao-Qin Li, Peng Liu, Jin-Wen Song, Xue Liu, Feng Xu, Jing Lei, Song He

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Other Types of Glycosylation.Advances in experimental medicine and biology · 2021
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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 4 institutions in 1 country.

Zhi-Hang Zhoua Department of Gastroenterology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Qing-Liang Wangc Department of Pathology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Lin-Hong Maoa Department of Gastroenterology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Xiao-Qin Lia Department of Gastroenterology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Peng Liud Department of Emergency , Chest Pain Center, General Hospital of Guangzhou Military Command , Guangzhou , China.
Jin-Wen Songe Treatment and Research Center for Infectious Diseases, The 302nd hosptital of PLA , Beijing , China.ORCID 0000-0002-8582-8012
Xue Liuf Department of Pathology , Basic Science School, Jining Medical University , Jining , Shandong , China.
Feng Xua Department of Gastroenterology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Jing Leia Department of Gastroenterology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Song Hea Department of Gastroenterology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.
Dalian Medical University · CN302 Military Hospital of China · CNGeneral Hospital of Guangzhou Military Command · CNJining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The acidic extracellular microenvironment, namely acidosis, is a biochemical hallmark of solid tumors. However, the tumorigenicity, metastatic potential, gene expression profile and chromatin accessibility of acidosis-adapted colorectal cancer cells remain unknown. The colorectal cancer cell SW620 was cultured in acidic medium (pH 6.5) for more than 3 months to be acidosis-adapted (SW620-AA). In comparison to parental cells, SW620-AA cells exhibit enhanced tumorigenicity and liver metastatic potential in vivo. Following mRNA and lncRNA expression profiling, we validated that OLMF1, NFIB, SMAD9, DGKB are upregulated, while SESN2, MAP1B, UTRN, PCDH19, IL18, LMO2, CNKSR3, GXYLT2 are downregulated in SW620-AA cells. The differentially expressed mRNAs were significantly enriched in DNA remodeling-associated pathways including HDACs deacetylate histones, SIRT1 pathway, DNA methylation, DNA bending complex, and RNA polymerase 1 chain elongation. Finally, chromatin accessibility evaluation by ATAC-sequencing revealed that the differentially opened peaks were enriched in pathways such as small cell lung cancer, pathways in cancer, ErbB signaling, endometrial cancer, and chronic myeloid leukemia, which were mainly distributed in intergenic regions and introns. These results suggest that the chromatin accessibility changes are correlated with enhanced growth and liver metastasis capacity of acid-adapted colorectal cancer cells.

Indexed as

AcidosisAnimalsCell Line, TumorChromatinChromatin Assembly and DisassemblyColorectal NeoplasmsCulture MediaGene Expression Regulation, NeoplasticHeterograftsHumansHydrogen-Ion ConcentrationLiver NeoplasmsMiceMice, Inbred BALB CMice, NudeRNA, Long NoncodingChromatinCulture MediaRNA, Long NoncodingRNA, Messengeracidosischromatin accessibilityColorectal cancermetastasisNFIB

Identifiers

PMID30712429
PMCPMC6422493
OpenAlexW2913451408

What OpenQuestion holds

Textmetadata
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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.