Evidence map›Paper›PMID 38596309›Full record

ArticleMolecular therapy. Oncology2024

Targeting the ribosome to treat multiple myeloma.

Kylee H Maclachlan, Kezia Gitareja, Jian Kang, Andrew Cuddihy, Yuxi Cao, Nadine Hein, Carleen Cullinane, Ching-Seng Ang, Natalie Brajanovski, Richard B Pearson and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Molecular therapy. Oncology, 2024. 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
3.6field-weighted citation impact, top 7% 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, 8 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Kylee H MaclachlanCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Kezia GitarejaSt Vincent's Institute of Medical Research, Melbourne, VIC, Australia.
Jian KangSt Vincent's Institute of Medical Research, Melbourne, VIC, Australia.
Andrew CuddihyCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Yuxi CaoCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Nadine HeinThe ACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia.
Carleen CullinaneCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Ching-Seng AngThe Bio21 Institute of Molecular Science and Biotechnology Institute, University of Melbourne, Melbourne, VIC, Australia.
Natalie BrajanovskiCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Richard B PearsonCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Amit KhotSir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.
Elaine SanijCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Ross D HannanThe ACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia.
Gretchen PoortingaCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Simon J HarrisonCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
The University of Melbourne · AUPeter MacCallum Cancer Centre · AUAustralian National University · AUBiotechnology Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high rates of protein synthesis and processing render multiple myeloma (MM) cells vulnerable to perturbations in protein homeostasis. The induction of proteotoxic stress by targeting protein degradation with proteasome inhibitors (PIs) has revolutionized the treatment of MM. However, resistance to PIs is inevitable and represents an ongoing clinical challenge. Our first-in-human study of the selective inhibitor of RNA polymerase I transcription of ribosomal RNA genes, CX-5461, has demonstrated a potential signal for anti-tumor activity in three of six heavily pre-treated MM patients. Here, we show that CX-5461 has potent anti-myeloma activity in PI-resistant MM preclinical models

Indexed as

CX-5461MT: Regular Issuemultiple myelomapanobinostatribosome biogenesisRNA polymerase I

Identifiers

PMID38596309
PMCPMC10905045
OpenAlexW4391605132

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.