Evidence map›Paper›PMID 27411517›Full record

ArticleBMC cancer2016

SOX2 expression is associated with a cancer stem cell state and down-regulation of CDX2 in colorectal cancer.

Ida V Lundberg, Sofia Edin, Vincy Eklöf, Åke Öberg, Richard Palmqvist, Maria L Wikberg

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 101 citations in OpenAlex.

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  20. β-carotene regulates cancer stemness in colon cancerNutrition research and practice · 2022
    Article
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 1 institution in 1 country.

Ida V LundbergDepartment of Medical Biosciences, Pathology, Umeå University, Building 6M, SE-90185, Umeå, Sweden.
Sofia EdinDepartment of Medical Biosciences, Pathology, Umeå University, Building 6M, SE-90185, Umeå, Sweden. sofia.edin@umu.se.
Vincy EklöfDepartment of Medical Biosciences, Pathology, Umeå University, Building 6M, SE-90185, Umeå, Sweden.
Åke ÖbergDepartment of Surgical and Perioperative Sciences, Surgery, Umeå University, Umeå, Sweden.
Richard PalmqvistDepartment of Medical Biosciences, Pathology, Umeå University, Building 6M, SE-90185, Umeå, Sweden.
Maria L WikbergDepartment of Medical Biosciences, Pathology, Umeå University, Building 6M, SE-90185, Umeå, Sweden.
Umeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo improve current treatment strategies for patients with aggressive colorectal cancer (CRC), the molecular understanding of subgroups of CRC with poor prognosis is of vast importance. SOX2 positive tumors have been associated with a poor patient outcome, but the functional role of SOX2 in CRC patient prognosis is still unclear.

methodsAn in vitro cell culture model expressing SOX2 was used to investigate the functional role of SOX2 in CRC. In vitro findings were verified using RNA from fresh frozen tumor tissue or immunohistochemistry on formalin fixed paraffin embedded (FFPE) tumor tissue from a cohort of 445 CRC patients.

resultsUsing our in vitro model, we found that SOX2 expressing cells displayed several characteristics of cancer stem cells; such as a decreased proliferative rate, a spheroid growth pattern, and increased expression of stem cell markers CD24 and CD44. Cells expressing SOX2 also showed down-regulated expression of the intestinal epithelial marker CDX2. We next evaluated CDX2 expression in our patient cohort. CDX2 down-regulation was more often found in right sided tumors of high grade and high stage. Furthermore, a decreased expression of CDX2 was closely linked to MSI, CIMP-high as well as BRAF mutated tumors. A decreased expression of CDX2 was also, in a stepwise manner, strongly correlated to a poor patient prognosis. When looking at SOX2 expression in relation to CDX2, we found that SOX2 expressing tumors more often displayed a down-regulated expression of CDX2. In addition, SOX2 expressing tumors with a down-regulated CDX2 expression had a worse patient prognosis compared to those with retained CDX2 expression.

conclusionsOur results indicate that SOX2 expression induces a cellular stem cell state in human CRC with a decreased expression of CDX2. Furthermore, a down-regulated expression of CDX2 results in a poor patient prognosis in CRC and at least part of the prognostic importance of SOX2 is mediated through CDX2 down-regulation.

Indexed as

AgedAged, 80 and overCaco-2 CellsCDX2 Transcription FactorCell MovementCell ProliferationCohort StudiesColorectal NeoplasmsCpG IslandsDNA MethylationDown-RegulationFemaleHumansImmunohistochemistryKaplan-Meier EstimateMaleBRAF protein, humanCDX2 protein, humanCDX2 Transcription FactorProto-Oncogene Proteins B-rafSOX2 protein, humanSOXB1 Transcription FactorsCancer stem cellCDX2Colorectal cancerPrognosisSOX2

Identifiers

PMID27411517
PMCPMC4944515
OpenAlexW2472105705

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.