Evidence map›Paper›PMID 26589512›Full record

ArticlePathology oncology research : POR2016

Prognostic Factors for Breast Cancer: an Immunomorphological Update.

Luca Roncati, Giuseppe Barbolini, Federico Piacentini, Francesco Piscioli, Teresa Pusiol, Antonio Maiorana

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 23 citations in OpenAlex.

  1. Observational
  2. Peripheral Blood CD8International journal of molecular sciences · 2024
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  4. 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

6 authors at 2 institutions in 1 country.

Luca RoncatiDepartment of Diagnostic and Clinical Medicine and of Public Health, Section of Pathology, University of Modena and Reggio Emilia, Policlinico Hospital, I-41124, Modena, (MO), Italy. emailmedical@gmail.com.
Giuseppe BarboliniDepartment of Diagnostic and Clinical Medicine and of Public Health, Section of Pathology, University of Modena and Reggio Emilia, Policlinico Hospital, I-41124, Modena, (MO), Italy.
Federico PiacentiniDepartment of Diagnostic and Clinical Medicine and of Public Health, Section of Oncology, University of Modena and Reggio Emilia, Modena, (MO), Italy.
Francesco PiscioliProvincial Health Care Services, Santa Maria del Carmine Hospital, Institute of Pathology, Rovereto, (TN), Italy.
Teresa PusiolProvincial Health Care Services, Santa Maria del Carmine Hospital, Institute of Pathology, Rovereto, (TN), Italy.
Antonio MaioranaDepartment of Diagnostic and Clinical Medicine and of Public Health, Section of Pathology, University of Modena and Reggio Emilia, Policlinico Hospital, I-41124, Modena, (MO), Italy.
University of Modena and Reggio Emilia · ITOspedale Santa Maria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognostic variability recorded within homogeneous groups of patients for anatomo-clinical disease stages has led to a more detailed biological characterization of breast cancer. Recently, the attention of the scientific community has focused on the role of tumor-infiltrating lymphocytes (TILs). Therefore, the need of an in-depth immunomorphological characterization of TILs has been emerged. The presence of TILs has been retrospectively investigated in 113 female cases of ductal carcinoma. An immunohistochemical investigation with CD3, CD4, CD8, CD20, CD56, granulysin, perforin-1, granzyme-B and TIA-1 was performed according to the standard procedures on all 17 cases with TILs evidence. TILs consisted of T and B lymphocytes: the prevalent population showed a T immunoprofile with a CD8-immunopositive killer subpopulation (Tk), close-linked to carcinomatous cells, and a CD4-immunopositive helper subpopulation (Th), inside the tumor. A time sequence (firstly T, then B) has been disclosed. Granulysin, perforin, granzyme-B and TIA-1 were expressed by Tk cells. The activated Tk cells secrete these mediators as a result of the binding to the tumor target cell, causing its lytic planned death. The cytotoxicity supported by Tk cells appears an important favorable prognostic factor. Therefore, a graduation system for TILs in breast cancer has been here proposed (absent, non-brisk, brisk).

Indexed as

AdultAgedAntigens, Differentiation, T-LymphocyteB-LymphocytesBreast NeoplasmsCarcinoma, DuctalCell DeathFemaleGranzymesHumansLymphocytes, Tumor-InfiltratingMiddle AgedPerforinPoly(A)-Binding ProteinsPrognosisRetrospective StudiesAntigens, Differentiation, T-LymphocyteGNLY protein, humanGranzymesPerforinPoly(A)-Binding ProteinsT-Cell Intracellular Antigen-1TIA1 protein, humanBreast cancerGranulysinHistologyImmunohistochemistryPrognostic factorsTumor-infiltrating lymphocytes (TILs)

Identifiers

PMID26589512
OpenAlexW2176767812

What OpenQuestion holds

Textmetadata
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.