Evidence map›Paper›PMID 32587829›Full record

ArticleFrontiers in oncology2020

Maspin as a Prognostic Marker for Early Stage Colorectal Cancer With Microsatellite Instability.

Atsushi Tanaka, Julia Y Wang, Jinru Shia, Yihua Zhou, Makiko Ogawa, Ronald C Hendrickson, David S Klimstra, Michael H A Roehrl

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  12. Proteome-based pathology: the next frontier in precision medicine.Expert review of precision medicine and drug development · 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

8 authors at 3 institutions in 3 countries.

Atsushi TanakaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Julia Y WangCurandis, New York, NY, United States.
Jinru ShiaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Yihua ZhouDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Makiko OgawaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Ronald C HendricksonMemorial Sloan Kettering Cancer Center, Sloan Kettering Institute, New York, NY, United States.
David S KlimstraDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Michael H A RoehrlDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Memorial Sloan Kettering Cancer Center · USNanchang University · CNThe University of Tokyo · JP

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Proteomic Characterization of Genomically Complex SarcomasR21CA251992 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ROEHRL, MICHAEL H. A. · 2020 to 2020
$487k
Targeting Multiple Colorectal Cancer-Specific EnhancersR21CA231109 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI PTASHNE, MARK S · 2019 to 2020
$430k
NCI NIH HHS P30 CA008748NCI NIH HHS R21 CA231109NCI NIH HHS R21 CA251992
6 · The paper itself

Abstract

Colorectal cancers are among the most common cancers and a leading cause of cancer death. In our pursuit to discover molecular markers for better characterization and precision theranostics of these cancers, we first conducted global deep proteome analyses and identified maspin (serpin B5, peptidase inhibitor 5) as an upregulated protein in tumor tissue. We then validated its expression in a large cohort of 743 patients with colorectal cancers of all stages and found that both cytoplasmic and nuclear expression varied widely between different patients. Comparison with clinicopathological features revealed that maspin expression levels correlate significantly only with mismatch repair (MMR) status but not with other features. To elucidate the prognostic significance of maspin, we analyzed two outcome-annotated cohorts, one of 572 early stage cancer patients and another of 93 late stage cancer patients. Kaplan-Meier survival, univariate, and multivariate analyses revealed that maspin overexpression predicts longer overall and disease-free survival for early stage microsatellite instability (MSI) subtype colorectal cancer, but there is no correlation with survival for patients with early stage cancer of the microsatellite stability (MSS) subtype or late stage cancer. Our study identifies maspin expression as an independent prognostic marker for risk stratification of early stage MSI subtype colorectal cancer and may provide guidance for improved therapeutic management.

Indexed as

biomarkercolorectal cancermaspinpathologyprognosisserpin B5

Identifiers

PMID32587829
PMCPMC7297950
OpenAlexW3034912387

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.