Evidence map›Paper›PMID 34481452›Full record

ArticleBMC gastroenterology2021

Elevated tumor expression of Astroprincin (FAM171A1) is an independent marker of poor prognosis in colon cancer.

Tuomas Kaprio, Alexander M Lindström, Tiina Rasila, Olga Saavalainen, Ines Beilmann-Lehtonen, Harri Mustonen, Caj Haglund, Leif C Andersson

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2021. 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
0.2field-weighted citation impact, top 50% 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. Article
  2. Increased Kremen2 predicts worse prognosis in colon cancer.Pathology oncology research : POR · 2023
    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 1 institution in 1 country.

Tuomas Kaprio *Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. tuomas.kaprio@helsinki.fi.ORCID http://orcid.org/0000-0002-0377-9975
Alexander M Lindström *Department of Pathology, University of Helsinki and Helsinki University Hospital, Haartmaninkatu 3 (PB 21), 00014, Helsinki, Finland.
Tiina RasilaDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Haartmaninkatu 3 (PB 21), 00014, Helsinki, Finland.
Olga SaavalainenDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Haartmaninkatu 3 (PB 21), 00014, Helsinki, Finland.
Ines Beilmann-LehtonenResearch Programs Unit, Translational Cancer Medicine, University of Helsinki, Helsinki, Finland.
Harri MustonenDepartment of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Caj Haglund *Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Leif C Andersson *Department of Pathology, University of Helsinki and Helsinki University Hospital, Haartmaninkatu 3 (PB 21), 00014, Helsinki, Finland.
University of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColon cancer (CC) is one of the most commonly diagnosed malignancies worldwide. Several biomarkers have been suggested for improved prognostic evaluation, but few have been implemented in clinical practice. There is a need for biomarkers that predict the tumor behavior in CC and allow stratification of patients that would benefit from adjuvant therapy. We recently identified and functionally characterized a previously unknown protein that we called ASTROPRINCIN (APCN) due to its abundance in astrocytes. APCN, also annotated as FAM171A1, is found in trophoblasts of early placenta. We demonstrated that high expression levels of APCN in cancer cells induced motility and ability of invasive growth in semisolid medium.

methodsWe screened by immunohistochemistry a tissue microarray material from the tumors of 429 CC patients with clinical follow-up in a test series and 255 CC patients in a validation series.

resultsWe showed that low or absent APCN expression correlates with a favorable prognosis while high APCN expression was a sign of an adverse outcome. Cox uni- and multivariable analysis revealed that elevated tumor expression of APCN constitutes a robust marker of poor prognosis independent of stage, grade, patient's age, or gender.

conclusionOur findings demonstrate that APCN is a novel independent prognostic marker in CC and could potentially select patients for more intense postoperative adjuvant treatment and follow-up.

Indexed as

Biomarkers, TumorColonic NeoplasmsHumansImmunohistochemistryPrognosisProteinsBiomarkers, TumorProteinsAstroprincinColon cancerFAM171A1ImmunohistochemistryTissue microarray

Identifiers

PMID34481452
PMCPMC8418715
OpenAlexW3196642552

What OpenQuestion holds

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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.