Evidence map›Paper›PMID 32019190›Full record

ReviewInternational journal of molecular sciences2020

Impact and Intricacies of Bone Marrow Microenvironment in B-cell Lymphomas: From Biology to Therapy.

Anuvrat Sircar, Sayan Mullick Chowdhury, Amber Hart, William Connor Bell, Satishkumar Singh, Lalit Sehgal, Narendranath Epperla

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Drug Resistance in Hematological Malignancies.International journal of molecular sciences · 2020
    Article
  11. Review
  12. Review
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 1 institution in 1 country.

Anuvrat SircarDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.
Sayan Mullick ChowdhuryDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.
Amber HartDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.
William Connor BellDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.
Satishkumar SinghDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.
Lalit SehgalDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0002-1151-5427
Narendranath EpperlaDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0002-8216-3457
The Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphoma, a group of widely prevalent hematological malignancies of lymphocyte origin, has become the focus of significant clinical research due to their high propensity for refractory/relapsed (R/R) disease, leading to poor prognostic outcomes. The complex molecular circuitry in lymphomas, especially in the aggressive phenotypes, has made it difficult to find a therapeutic option that can salvage R/R disease. Furthermore, the association of lymphomas with the Bone Marrow (BM) microenvironment has been found to portend worse outcomes in terms of heightened chances of relapse and acquired resistance to chemotherapy. This review assesses the current therapy options in three distinct types of lymphomas: diffuse large B-cell lymphoma, follicular lymphoma and mantle cell lymphoma. It also explores the role of the BM tumor microenvironment as a secure 'niche' for lymphoma cells to grow, proliferate and survive. It further evaluates potential mechanisms through which the tumor cells can establish molecular connections with the BM cells to provide pro-tumor benefits, and discusses putative therapeutic strategies for disrupting the BM-lymphoma cell communication.

Indexed as

Drug Resistance, NeoplasmAntineoplastic Combined Chemotherapy ProtocolsBone MarrowHumansLymphoma, B-CellTumor Microenvironmentbone marrow microenvironmentdiffuse large B-cell lymphomadrug resistancefollicular lymphomamantle cell lymphomarelapse

Identifiers

PMID32019190
PMCPMC7043222
OpenAlexW3003192513

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.