Evidence map›Paper›PMID 33634031›Full record

ReviewFrontiers in oncology2020

Game of Bones: How Myeloma Manipulates Its Microenvironment.

Tyler Moser-Katz, Nisha S Joseph, Madhav V Dhodapkar, Kelvin P Lee, Lawrence H Boise

Open access · goldAbstract readReview
In one paragraph

Review 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 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.8field-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

38 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Talazoparib and radiation enhance the senolytic efficacy of venetoclax in therapy-induced senescent triple-negative breast cancer cells.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Endogenous CD28 drives CAR T cell responses in multiple myeloma.bioRxiv : the preprint server for biology · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Epigenetic effects of herbal medicine.Clinical epigenetics · 2023
    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

5 authors at 2 institutions in 1 country.

Tyler Moser-KatzDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Nisha S JosephDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Madhav V DhodapkarDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Kelvin P LeeDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY, United States.
Lawrence H BoiseDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Emory University · USRoswell Park Comprehensive Cancer Center · US

Funding

The Role of CD86 in Multiple MyelomaR01CA192844 · NCI · EMORY UNIVERSITY · PI BOISE, LAWRENCE H. · 2016 to 2020
$1.9M
NCI NIH HHS R01 CA192844
6 · The paper itself

Abstract

Multiple myeloma is a clonal disease of long-lived plasma cells and is the second most common hematological cancer behind Non-Hodgkin's Lymphoma. Malignant transformation of plasma cells imparts the ability to proliferate, causing harmful lesions in patients. In advanced stages myeloma cells become independent of their bone marrow microenvironment and form extramedullary disease. Plasma cells depend on a rich array of signals from neighboring cells within the bone marrow for survival which myeloma cells exploit for growth and proliferation. Recent evidence suggests, however, that both the myeloma cells and the microenvironment have undergone alterations as early as during precursor stages of the disease. There are no current therapies routinely used for treating myeloma in early stages, and while recent therapeutic efforts have improved patients' median survival, most will eventually relapse. This is due to mutations in myeloma cells that not only allow them to utilize its bone marrow niche but also facilitate autocrine pro-survival signaling loops for further progression. This review will discuss the stages of myeloma cell progression and how myeloma cells progress within and outside of the bone marrow microenvironment.

Indexed as

bone marrow microenviromentMGUSmultiple myelomamyeloma therapysmoldering myeloma

Identifiers

PMID33634031
PMCPMC7900622
OpenAlexW3128568012

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.