Evidence map›Paper›PMID 39062846›Full record

ReviewInternational journal of molecular sciences2024

Deciphering Drug Resistance: Investigating the Emerging Role of Hyaluronan Metabolism and Signaling and Tumor Extracellular Matrix in Cancer Chemotherapy.

Daiana L Vitale, Arianna Parnigoni, Manuela Viola, Evgenia Karousou, Ina Sevic, Paola Moretto, Alberto Passi, Laura Alaniz, Davide Vigetti

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
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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

9 authors.

Daiana L VitaleLaboratorio de Microambiente Tumoral, Centro de Investigaciones Básicas y Aplicadas (CIBA), Universidad Nacional del Noroeste de la Provincia de Buenos Aires, Junín B6000, Argentina.
Arianna ParnigoniDepartment of Medical Biochemistry and Microbiology, Uppsala University, SE-751 23 Uppsala, Sweden.
Manuela ViolaDipartimento di Medicina e Chirurgia, Universitá degli Studi dell'Insubria, 21100 Varese, Italy.ORCID 0000-0002-0634-6390
Evgenia KarousouDipartimento di Medicina e Chirurgia, Universitá degli Studi dell'Insubria, 21100 Varese, Italy.
Ina SevicLaboratorio de Microambiente Tumoral, Centro de Investigaciones Básicas y Aplicadas (CIBA), Universidad Nacional del Noroeste de la Provincia de Buenos Aires, Junín B6000, Argentina.
Paola MorettoDipartimento di Medicina e Chirurgia, Universitá degli Studi dell'Insubria, 21100 Varese, Italy.
Alberto PassiDipartimento di Medicina e Chirurgia, Universitá degli Studi dell'Insubria, 21100 Varese, Italy.
Laura AlanizLaboratorio de Microambiente Tumoral, Centro de Investigaciones Básicas y Aplicadas (CIBA), Universidad Nacional del Noroeste de la Provincia de Buenos Aires, Junín B6000, Argentina.ORCID 0000-0002-6070-6078
Davide VigettiDipartimento di Medicina e Chirurgia, Universitá degli Studi dell'Insubria, 21100 Varese, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyaluronan (HA) has gained significant attention in cancer research for its role in modulating chemoresistance. This review aims to elucidate the mechanisms by which HA contributes to chemoresistance, focusing on its interactions within the tumor microenvironment. HA is abundantly present in the extracellular matrix (ECM) and binds to cell-surface receptors such as CD44 and RHAMM. These interactions activate various signaling pathways, including PI3K/Akt, MAPK, and NF-κB, which are implicated in cell survival, proliferation, and drug resistance. HA also influences the physical properties of the tumor stroma, enhancing its density and reducing drug penetration. Additionally, HA-mediated signaling contributes to the epithelial-mesenchymal transition (EMT), a process associated with increased metastatic potential and resistance to apoptosis. Emerging therapeutic strategies aim to counteract HA-induced chemoresistance by targeting HA synthesis, degradation, metabolism, or its binding to CD44. This review underscores the complexity of HA's role in chemoresistance and highlights the potential for HA-targeted therapies to improve the efficacy of conventional chemotherapeutics.

Indexed as

Drug Resistance, NeoplasmEpithelial-Mesenchymal TransitionExtracellular MatrixHyaluronic AcidNeoplasmsSignal TransductionTumor MicroenvironmentAnimalsAntineoplastic AgentsHumansHyaluronan ReceptorsAntineoplastic AgentsHyaluronan ReceptorsHyaluronic Acid4-MUchemotherapydrug resistanceHAS2HAS2-AS1hyaluronanUGDH

Identifiers

PMID39062846
PMCPMC11276752

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.