Evidence map›Paper›PMID 31934533›Full record

ReviewAnalytical cellular pathology (Amsterdam)2019

Tumor Microenvironment in Diffuse Large B-Cell Lymphoma: Role and Prognosis.

Alexandra Ioana Cioroianu, Patricia Irina Stinga, Liana Sticlaru, Mirela Daniela Cioplea, Luciana Nichita, Cristiana Popp, Florica Staniceanu

Open access · goldAbstract readReview
In one paragraph

Review in Analytical cellular pathology (Amsterdam), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 94 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

13 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Alexandra Ioana CioroianuDepartment of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.ORCID https://orcid.org/0000-0002-7152-3744
Patricia Irina StingaDepartment of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
Liana SticlaruDepartment of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
Mirela Daniela CiopleaDepartment of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
Luciana NichitaDepartment of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
Cristiana PoppDepartment of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.ORCID https://orcid.org/0000-0001-8579-4986
Florica StaniceanuFaculty of Dental Medicine, University of Medicine and Pharmacy "Carol Davila", 020021 Bucharest, Romania.
Spitalul Clinic Colentina · ROCarol Davila University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL) represents 30-40% of all non-Hodgkin lymphomas (NHL) and is a disease with an aggressive behavior. Because about one-third of DLBCL patients will be refractory or resistant to standard therapy, several studies focused on identification of new individual prognostic and risk stratification biomarkers and new potential therapeutic targets. In contrast to other types of cancers like carcinomas, where tumor microenvironment was widely investigated, its role in DLBCL pathogenesis and patient survival is still poorly understood, although few studies had promising results. The composition of TME and its interaction with neoplastic cells may explain the role of several genes (beta2-microglobulin gene, CD58 gene), receptor-like programmed cell death-1 (PD-1) and its ligand (PD-L1), or other cell components (Treg) in tumor evasion of immune surveillance, resulting in tumor progression. Also, it was found that "gene expression profile" of the microenvironmental cells, the phenotype of tumor-associated macrophages (TAM), the expression of matricellular proteins like SPARC and fibronectin, the overexpression of several types of matrix metalloproteinases (MMPs) like MMP-2 and MMP-9, or the tissue inhibitors of matrix metalloproteinases (TIMPs) may lead to a favorable or adverse outcome. With this review, we try to highlight the influence of microenvironment components over lymphoid clone progression and their prognostic impact in DLBCL patients.

Indexed as

B7-H1 AntigenBiomarkers, TumorExtracellular MatrixHumansLymphoma, Large B-Cell, DiffuseMacrophagesNeovascularization, PathologicPrognosisProgrammed Cell Death 1 ReceptorTumor MicroenvironmentB7-H1 AntigenBiomarkers, TumorCD274 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID31934533
PMCPMC6942707
OpenAlexW2996065673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.