Evidence map›Paper›PMID 30980190›Full record

ArticleVirchows Archiv : an international journal of pathology2019

CD70 expression in tumor-associated fibroblasts predicts worse survival in colorectal cancer patients.

Satoshi Inoue, Hideaki Ito, Takumi Tsunoda, Hideki Murakami, Masahide Ebi, Naotaka Ogasawara, Kunio Kasugai, Kenji Kasai, Hiroshi Ikeda, Shingo Inaguma

Abstract read
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

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  12. Efficacy of bivalentHeliyon · 2022
    Article
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  15. SPATA18 Expression Predicts Favorable Clinical Outcome in Colorectal Cancer.International journal of molecular sciences · 2022
    Article
  16. The CD70-CD27 axis in oncology: the new kids on the block.Journal of experimental & clinical cancer research : CR · 2022
    Review
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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 1 institution in 1 country.

Satoshi InoueDivision of Gastroenterology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute, Japan.
Hideaki ItoDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Takumi TsunodaDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Hideki MurakamiDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Masahide EbiDivision of Gastroenterology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute, Japan.
Naotaka OgasawaraDivision of Gastroenterology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute, Japan.
Kunio KasugaiDivision of Gastroenterology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute, Japan.
Kenji KasaiDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Hiroshi IkedaDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Shingo InagumaDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan. inaguma@aichi-med-u.ac.jp.ORCID http://orcid.org/0000-0001-8585-8900
Aichi Medical University · JP

Funding

Japan Society for the Promotion of Science 17K08706
6 · The paper itself

Abstract

The anticancer effects of immune checkpoint inhibitors against CTLA4 and CD274-PDCD1 axes are evident. However, these immunotherapies for colorectal cancers (CRCs) are now limited to a small subset of patients with microsatellite unstable tumors. Thus, therapeutics targeting other types of CRCs is desired. The CD70-CD27 axis plays a co-stimulatory role in promoting the expansion and differentiation of T-lymphocytes through the activation of NFκB pathway. Aberrant activation of the CD70-CD27 axis accelerates tumor cell proliferation, survival, and immune evasion of tumor cells. Based on these observations, drugs modulating the CD70-CD27 axis have been developed with expectation of anticancer effects. In the present study, 269 primary CRCs were evaluated immunohistochemically for CD70, CD27, and FOXP3 expression to assess their clinical usage and the application of CD70-CD27 axis modulating drugs. CRC tumor cells rarely (2.2%) expressed CD70. In contrast, tumor-surrounding fibroblasts showed various CD70 expressions (fCD70) in 14.9%. The logistic regression analysis revealed significant association of fCD70 expression with incomplete resection status (OR, 2.60; 95% CI, 1.10-6.13; P = 0.029). Overall survival was significantly decreased in the cohort of the patients with fCD70-positive tumor (P = 0.0078). Furthermore, significantly more CD27+ tumor-associated lymphocytes were detected within the primary CRCs without metastases (P = 0.024). Thus, the CD70-CD27 axis may have several roles in CRCs independent from their mismatch repair (MMR) system status. CD70-CD27 pathway-modulating therapies may be applied to CRC patients regardless of their tumor MMR status.

Indexed as

AdultAgedBiomarkers, TumorCancer-Associated FibroblastsCD27 LigandColorectal NeoplasmsFemaleHumansMaleMiddle AgedTumor Necrosis Factor Receptor Superfamily, Member 7Biomarkers, TumorCD27 LigandCD70 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 7CD27CD70Colorectal cancer (CRC)FOXP3Immunohistochemistry

Identifiers

PMID30980190
OpenAlexW2936562705

What OpenQuestion holds

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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.