Evidence map›Paper›PMID 35221802›Full record

ArticlePathology oncology research : POR2022

Expression and Potential Prognostic Value of SOX9, MCL-1 and SPOCK1 in Gastric Adenocarcinoma.

Wenyi Luo, Teddy S Nagaria, Hongxia Sun, Junsheng Ma, Jamie L Lombardo, Roland Bassett, Austin C Cao, Dongfeng Tan

Open access · goldAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 2 institutions in 2 countries.

Wenyi LuoDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.
Teddy S NagariaDepartment of Pathology and Laboratory Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Hongxia SunDepartment of Pathology and Laboratory Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Junsheng MaDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Jamie L LombardoDepartment of Pathology and Laboratory Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Roland BassettDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Austin C CaoPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Dongfeng TanDepartment of Pathology and Laboratory Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
The University of Texas MD Anderson Cancer Center · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer is a common malignancy and remains one of the leading causes of cancer-related deaths, though its incidence is in decline in most developed countries. One of the major challenges of treating gastric cancer is tumor heterogeneity, which portends a high degree of prognostic variance and the necessity for different treatment modalities. Tumor heterogeneity is at least in part due to divergent differentiation of tumor cells to clones harboring different molecular alterations. Here we studied the expression of emerging prognostic markers SOX9, MCL-1, and SPOCK1 (Testican-1) in a cohort of gastric cancer by immunohistochemistry and investigated how individual biomarkers and their combinations predict disease prognosis. We found frequent expression of SPOCK1 (in both nuclei and cytoplasm), MCL-1 and SOX9 in gastric cancer. In univariate analysis, nuclear SPOCK1 expression and pathologic TNM stage were negative prognostic markers in this cohort. In multivariate analysis, SOX9 expression stood out as a predictor of poor prognosis. Further subgroup analysis suggested prognostic value of SOX9 expression in poorly differentiated gastric adenocarcinoma. MCL-1 showed no prognostic role in this cohort.

Indexed as

AdenocarcinomaStomach NeoplasmsBiomarkers, TumorHumansImmunohistochemistryMyeloid Cell Leukemia Sequence 1 ProteinPrognosisProteoglycansSOX9 Transcription FactorBiomarkers, TumorMCL1 protein, humanMyeloid Cell Leukemia Sequence 1 ProteinProteoglycansSOX9 protein, humanSOX9 Transcription FactorSPOCK1 protein, humangastric cancerMCL-1prognosisSOX9SPOCK1

Identifiers

PMID35221802
PMCPMC8863590
OpenAlexW4211214656

What OpenQuestion holds

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LicenceCC BY
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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.