Evidence map›Paper›PMID 31089242›Full record

ArticleScientific reports2019

The HuR CMLD-2 inhibitor exhibits antitumor effects via MAD2 downregulation in thyroid cancer cells.

Lorenzo Allegri, Federica Baldan, Sudeshna Roy, Jeffrey Aubé, Diego Russo, Sebastiano Filetti, Giuseppe Damante

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Regulation of RNA-binding proteins by small biomolecules.Nature reviews. Molecular cell biology · 2026
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  7. HuR inhibition reduces post-ischemic cardiac remodeling by dampening myocyte-dependent inflammatory gene expression and the innate immune response.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  8. Review
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  10. Article
  11. Review
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  14. Article
  15. Review
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  18. Relationship between HuR and tumor drug resistance.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  19. Article
  20. 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

7 authors at 5 institutions in 2 countries.

Lorenzo AllegriDepartment of Medical Area, University of Udine, 33100, Udine, Italy.
Federica BaldanDepartment of Translational and Precision Medicine, University of Roma 'Sapienza', 06100, Roma, Italy. federica.baldan12@gmail.com.
Sudeshna RoyDepartment of BioMelecular Sciences, School of Pharmacy, University of Mississippi, 413 Faser Hall, Mississippi, 38677-1848, USA.
Jeffrey AubéDivision of Chemical Biology and Medical Chemistry, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, North Carolina, 27599-7363, USA.
Diego RussoDepartment of Health Sciences, University of Catanzaro "Magna Graecia", 88100, Catanzaro, Italy.
Sebastiano FilettiDepartment of Translational and Precision Medicine, University of Roma 'Sapienza', 06100, Roma, Italy.
Giuseppe DamanteDepartment of Medical Area, University of Udine, 33100, Udine, Italy.
Sapienza University of Rome · ITUniversity of Udine · ITMagna Graecia University · ITUniversity of Mississippi · USUniversity of North Carolina at Chapel Hill · US

Funding

Molecular cancer therapy targeting HuR-ARE interactionR01CA191785 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI AUBE, JEFFREY, XU, LIANG · 2015 to 2019
$2.1M
NCI NIH HHS R01 CA191785
6 · The paper itself

Abstract

Hu antigen R (HuR) is indeed one of the most studied RNA-binding protein (RBP) since its fundamental role both in tumorigenesis and cancer progression. For this reason, downregulation in HuR protein levels or inhibition of HuR biological function are, nowadays, attractive goals in cancer research. Here, we examined the antitumor effects of CMLD-2 in four thyroid cancer cell lines (SW1736, 8505 C, BCPAP and K1). Indeed, CMLD-2 competitively binds HuR protein disrupting its interaction with RNA-targets. 35 μM CLMD-2 produced a significant downregulation in thyroid cancer cell viability, coupled to an increase in apoptosis. Moreover, CMLD-2 treatment hindered both migration and colony formation ability. MAD2 is a microtubules-associated protein known to be greatly overexpressed in cancer and correlating with tumor aggressiveness. Furthermore, MAD2 is known to be a HuR target. CMLD-2 treatment induced a strong MAD2 downregulation and rescue experiments depicted it as a key effector in HuR-mediated in cancer. Altogether, these data contributed to foster HuR inhibition as valid antineoplastic treatment in thyroid cancer, highlighting MAD2 as a novel therapeutic target.

Indexed as

Antineoplastic AgentsBenzopyransCell Line, TumorCell MovementDown-RegulationELAV-Like Protein 1Gene Expression Regulation, NeoplasticHumansMad2 ProteinsPyrrolidinesThyroid NeoplasmsAntineoplastic AgentsBenzopyransCMLD-2ELAVL1 protein, humanELAV-Like Protein 1MAD2L1 protein, humanMad2 ProteinsPyrrolidines

Identifiers

PMID31089242
PMCPMC6517587
OpenAlexW2947329869

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.