Evidence map›Paper›PMID 40703048›Full record

ArticleIntegrative cancer therapies

Cannabinoid Derived Product is a Potential Novel Therapeutic for Papillary Thyroid Carcinoma.

Carolina Taico Oliva, Ibrahim Musa, Fariba Ardalani, Joseph Breslin, Nan Yang, Augustine Moscatello, Janine Rotsides, Raj Tiwari, Jan Geliebter, Xiu-Min Li

Abstract read
In one paragraph

Article in Integrative cancer therapies. 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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1 · What the graph read from it

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2 · The registry

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Carolina Taico OlivaNew York Medical College, Valhalla, USA.
Ibrahim MusaNew York Medical College, Valhalla, USA.ORCID 0000-0001-9309-9430
Fariba ArdalaniNew York Medical College, Valhalla, USA.
Joseph BreslinBreslin Research Foundation, Taos, NM, USA.
Nan YangGeneral Nutraceutical Technology LLC, Elmsford, NY, USA.
Augustine MoscatelloNew York Medical College, Valhalla, USA.
Janine RotsidesNew York Medical College, Valhalla, USA.
Raj TiwariNew York Medical College, Valhalla, USA.
Jan GeliebterNew York Medical College, Valhalla, USA.
Xiu-Min LiNew York Medical College, Valhalla, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationalePapillary thyroid carcinoma (PTC) is the most common thyroid cancer that typically affects women ages 20 to 50, presenting as an asymptomatic neck mass. Treatment with total or partial thyroidectomy shows an excellent prognosis. However, investigation of non-invasive therapeutic options with minimal adverse effects is ongoing. This study seeks to investigate the K1 cell line, which consists of PTC cells obtained from metastatic tumors of well-differentiated PTC.

objectiveOur investigation focuses on a cannabinoid-based product (named BRF1-A) and its potential anti-cancer effects through modulation of gene expression. We investigated its effects on gene expression of p53, c-Myc, and BCL-2 in K1 papillary thyroid cancer cells.

methodsBRF1A was co-cultured with K1 cell line (1 × 10

resultsResults show that the BRF1A decreased the viability of K1 PTC cells in a dose and time-dependent manner. Within 24 hours, the cannabinoid- containing product increased the gene expression of TP53 and decreased the gene expression of BCL-2 and c-Myc in K1 PTC cells.

conclusionThe results suggest that the cannabinoid-containing product BRF1A interacts as a potential regulator in well-differentiated thyroid cancer with the upregulation of p53 and downregulation of BLC-2 and c-Myc. Further in vitro and in vivo studies are needed to understand the exact mechanism and therapeutic potential of the cannabinoid-containing products in papillary thyroid cancer.

Indexed as

CannabinoidsThyroid Cancer, PapillaryThyroid NeoplasmsCell Line, TumorCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticHumansProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycTumor Suppressor Protein p53CannabinoidsMYC protein, humanProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycTumor Suppressor Protein p53cancer suppressor genescannabidiolcannabinolsenescencetetrahydrocannabinol

Identifiers

PMID40703048
PMCPMC12301603

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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.