Evidence map›Paper›PMID 32095781›Full record

ArticleFASEB bioAdvances2019

The snoRNA target of t(4;14) in multiple myeloma regulates ribosome biogenesis.

Vanessa Oliveira, Nitin Mahajan, Melissa L Bates, Chakrapani Tripathi, Kyusik Q Kim, Hani S Zaher, Leonard B Maggi, Michael H Tomasson

Open access · goldAbstract read
In one paragraph

Article in FASEB bioAdvances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Small nucleolar RNAs: the hidden precursors of cancer ribosomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  3. Review
  4. SnoRNAs: The promising targets for anti-tumor therapy.Journal of pharmaceutical analysis · 2024
    Review
  5. Article
  6. BRD9 Degradation Disrupts Ribosome Biogenesis in Multiple Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. 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

8 authors at 2 institutions in 1 country.

Vanessa OliveiraDivision of Hematology, Oncology and Bone Marrow Transplantation Department of Internal Medicine, University of Iowa, Iowa City, IA, USA.
Nitin MahajanDivision of Oncology, Department of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Melissa L BatesDepartment of Health and Human Physiology, USA.
Chakrapani TripathiDivision of Hematology, Oncology and Bone Marrow Transplantation Department of Internal Medicine, University of Iowa, Iowa City, IA, USA.
Kyusik Q KimDepartment of Biology, Washington University, St. Louis, Missouri, USA.
Hani S ZaherDepartment of Biology, Washington University, St. Louis, Missouri, USA.
Leonard B MaggiDivision of Oncology, Department of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Michael H TomassonDivision of Hematology, Oncology and Bone Marrow Transplantation Department of Internal Medicine, University of Iowa, Iowa City, IA, USA.
University of Iowa · USWashington University in St. Louis · US

Funding

Project 2 - Radiation-Induced Treatment of Multiple Myeloma using NanoparticlesU54CA199092 · NCI · WASHINGTON UNIVERSITY · PI ACHILEFU, SAMUEL · 2015 to 2019
$11.5M
MOLECULAR TARGETS OF TRANSLOCATION T(4;14) IN MULTIPLE MYELOMA PATHOGENESISR01CA175349 · NCI · WASHINGTON UNIVERSITY · PI TOMASSON, MICHAEL H · 2014 to 2018
$1.6M
ROLE OF ACA11, AN ORPHAN SMALL NUCLEOLAR RNA IN RESISTANCE TO CANCER CHEMOTHERAPYR01CA174743 · NCI · WASHINGTON UNIVERSITY · PI MAGGI, LEONARD B, TOMASSON, MICHAEL H · 2013 to 2017
$1.6M
NCI NIH HHS R01 CA174743NCI NIH HHS R01 CA175349NCI NIH HHS U54 CA199092
6 · The paper itself

Abstract

The orphan small nucleolar RNA (snoRNA) ACA11 is overexpressed as a result of the t(4;14) chromosomal translocation in multiple myeloma (MM), increases reactive oxygen species, and drives cell proliferation. Like other snoRNAs, ACA11 is predominantly localized to a sub-nuclear organelle, the nucleolus. We hypothesized that increased ACA11 expression would increase ribosome biogenesis and protein synthesis. We found that ACA11 overexpression in MM cells increased nucleolar area and number as well as silver-binding nucleolar organizing regions (AgNORs). Supporting these data, samples from t(4;14)-positive patients had higher AgNORs scores than t(4;14)-negative samples. ACA11 also upregulated ribosome production, pre-47S rRNA synthesis, and protein synthesis in a ROS-dependent manner. Lastly, ACA11 overexpression enhanced the response to proteasome inhibitor in MM cells, while no effect was found in response to high doses of melphalan. Together, these data demonstrate that ACA11 stimulates ribosome biogenesis and influences responses to chemotherapy. ACA11 may be a useful target to individualize the treatment for t(4;14)-positive myeloma patients.

Indexed as

chromosomal translocationhematological malignancyProtein synthesisreactive oxygen species

Identifiers

PMID32095781
PMCPMC6996358
OpenAlexW2937706807

What OpenQuestion holds

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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.