Evidence map›Paper›PMID 41945932›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2026

Chemotherapy Supports Cancer Cell Dissemination in a Melanoma Preclinical Model.

Ekaterina Lapkina, Tatiana Ruksha

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Ekaterina LapkinaDepartment of Pathophysiology, Krasnoyarsk State Medical University, P. Zeleznyaka str., 1, 660022, Krasnoyarsk, Russia.
Tatiana RukshaDepartment of Pathophysiology, Krasnoyarsk State Medical University, P. Zeleznyaka str., 1, 660022, Krasnoyarsk, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of the study was to determine how the chemotherapeutic alkylating agent dacarbazine, together with the application of the miR-204-5p mimic in vivo, affects the presence of disseminated melanoma cells in distant organs - the lungs and liver.

methodsThe study was carried out on B16 melanoma-bearing mice (n = 48). The animals were treated with dacarbazine (50 mg/kg) or dacarbazine combined with the microRNA miR-204-5p mimic (5 nM). Real-time PCR was used to evaluate the expression of miR-204-5p target genes following miR-204-5p mimic application. The presence of melanoma cells in distant organs was assessed by immunovisualization of the melanocyte marker PMEL using an immunohistochemical assay and by evaluating the expression of the melanocyte-specific protein tyrosinase via real-time PCR.

resultThe level of PMEL expression increased twofold in the lungs of mice treated with dacarbazine (p = 0.014) and 4.2-fold in the group of animals treated with a combination of dacarbazine and the miR-204-5p mimic (p = 0.001), as compared to the control group. However, tyrosinase expression was detected in the lungs of B16 melanoma-bearing mice treated with dacarbazine and the negative control only, due to the sporadic presence of melanoma cells in distant organs.

conclusionTaken together, dacarbazine and the miR-204-5p mimic favor the dissemination of B16 melanoma cells in the lungs, which may support further metastatic development. Although miR-204-5p has been described as a tumor-suppressive microRNA in melanoma, the application of a synthetic mimic to overexpress it in distant organs promoted tumor cell dissemination.

Indexed as

Antineoplastic Agents, AlkylatingDacarbazineLung NeoplasmsMelanoma, ExperimentalMicroRNAsAnimalsGene Expression Regulation, NeoplasticMiceMice, Inbred C57BLAntineoplastic Agents, AlkylatingDacarbazineMicroRNAsDacarbazinedisseminated cancer cellsMelanomaMetastasismiR-204-5p

Identifiers

PMID41945932
PMCPMC13609154

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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.