Evidence map›Paper›PMID 27392434›Full record

ArticleDiagnostic pathology2016

In depth evaluation of the prognostic and predictive utility of PTEN immunohistochemistry in colorectal carcinomas: performance of three antibodies with emphasis on intracellular and intratumoral heterogeneity.

Emese Irma Ágoston, Tamás Micsik, Balázs Ács, Krisztina Fekete, Oszkár Hahn, Zsolt Baranyai, Kristóf Dede, György Bodoky, Attila Bursics, Janina Kulka and 4 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Precise Immunodetection of PTEN Protein in Human Neoplasia.Cold Spring Harbor perspectives in medicine · 2019
    Review
  4. Review
  5. 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

14 authors at 3 institutions in 1 country.

Emese Irma ÁgostonDepartment of Surgery, Semmelweis University, 78 Üllői út, Budapest, 1082, Hungary.
Tamás MicsikDepartment of Pathology and Experimental Cancer Research, Semmelweis University, 26 Üllői út, Budapest, 1085, Hungary.
Balázs ÁcsDepartment of Pathology, Semmelweis University, 93 Üllői út, Budapest, 1091, Hungary.
Krisztina FeketeDepartment of Surgery, Semmelweis University, 78 Üllői út, Budapest, 1082, Hungary.
Oszkár HahnDepartment of Surgery, Semmelweis University, 78 Üllői út, Budapest, 1082, Hungary.
Zsolt BaranyaiDepartment of Surgery, Semmelweis University, 78 Üllői út, Budapest, 1082, Hungary.
Kristóf DedeDepartment of Surgery and Oncological Surgery, Uzsoki Teaching Hospital, 196 Róna utca, Budapest, 1145, Hungary.
György BodokyDepartment of Oncology, Szent István Hospital, 1 Nagyvárad tér, Budapest, 1097, Hungary.
Attila BursicsDepartment of Surgery and Oncological Surgery, Uzsoki Teaching Hospital, 196 Róna utca, Budapest, 1145, Hungary.
Janina KulkaDepartment of Pathology, Semmelweis University, 93 Üllői út, Budapest, 1091, Hungary.
Tibor KrenácsDepartment of Pathology and Experimental Cancer Research, Semmelweis University, 26 Üllői út, Budapest, 1085, Hungary.
Balázs GyőrffyMTA-TTK Lendület Cancer Biomarker Research Group, Magyar tudósok körútja 2, Budapest, 1117, Hungary.
László HarsányiDepartment of Surgery, Semmelweis University, 78 Üllői út, Budapest, 1082, Hungary. hl@seb1.sote.hu.
A Marcell SzászDepartment of Pathology, Semmelweis University, 93 Üllői út, Budapest, 1091, Hungary. cac@korb2.sote.hu.
Semmelweis University · HUHUN-REN Research Centre for Natural Sciences · HUUzsoki Hospital · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhosphatase and tensin homolog deleted in chromosome 10 (PTEN) loss of function is frequently detected in advanced colorectal cancer. Its detection is thought to have prognostic significance and it is being considered to predict responsiveness to anti-EGFR therapy. Unfortunately, while immunohistochemical assessment of PTEN expression is widespread, it lacks standardization and the results are hardly comparable across the available publications.

methodsRetrospectively collected, formalin-fixed and paraffin-embedded colorectal tumor tissue samples from 55 patients were combined into tissue microarray (TMA) blocks. We used three different PTEN antibodies to determine the frequency, intensity and intracellular pattern of PTEN immunohistochemical labeling: Neomarkers, Dako and CellSignaling. We evaluated the aforementioned parameters in selected regions of colorectal cancers and in their lymph node metastases by using three scoring methods that take into consideration both staining frequency and intensity (H1-H3-score). We also evaluated intracellular localization.

resultsThe Dako and CellSignaling antibodies stained predominantly cytoplasms, while the Neomarkers antibody specifically stained cell nuclei. PTEN H-scores were significantly lower in all tumor areas as compared to the normal colonic mucosa based on staining with the DAKO and CellSignaling antibodies. Intratumoral regional differences or differences between matching tumors and metastases were not detected with any of the antibodies. Neither Dako, neither CellSignaling, nor the Neomarkers antibodies revealed a significant correlation between PTEN expression and pT, Dukes/MAC and clinical stage. KRAS status, histological grade correlated with PTEN H-scores based on staining with the Neomarkers antibody. PTEN H-scores did not correlate with MMR status. PTEN H-scores did not show any correlation with relapse-free survival based on staining with either antibody.

conclusionsWhile PTEN expression decreased in colorectal cancer according to two antibodies, neither of the three applied PTEN antibodies could justify significant correlation with clinicopathological data, nor had prognostic value. Thus, we might conclude that immunohistochemical PTEN investigation remains a challenge requiring more standardized evaluation on larger number of cases to clarify its utility as a prognostic and predictive tool in CRC. The standardization of immunohistochemical method is key in the evaluation process, which is further discussed.

Indexed as

AgedAntibodies, MonoclonalBiomarkers, TumorColonColorectal NeoplasmsFemaleHumansImmunohistochemistryMaleMiddle AgedMutationNeoplasm StagingPredictive Value of TestsPrognosisProto-Oncogene Proteins p21(ras)PTEN PhosphohydrolaseAntibodies, MonoclonalBiomarkers, TumorKRAS protein, humanProto-Oncogene Proteins p21(ras)PTEN PhosphohydrolasePTEN protein, humanColorectal cancerImmunohistochemistryIntratumoral heterogeneityPredictive markerPrognostic markerProtein expressionPTEN

Identifiers

PMID27392434
PMCPMC4939017
OpenAlexW2467790384

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.