Evidence map›Paper›PMID 37569564›Full record

ArticleInternational journal of molecular sciences2023

The Effects of a Curcumin Derivative and Osimertinib on Fatty Acyl Metabolism and Mitochondrial Functions in HCC827 Cells and Tumors.

Min-Tsang Hsieh, Pei-Chih Lee, Yi-Ting Chiang, Hui-Yi Lin, Der-Yen Lee

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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

5 authors at 1 institution in 1 country.

Min-Tsang HsiehDrug Development Center, China Medical University, Taichung 406040, Taiwan.ORCID 0000-0001-7287-9278
Pei-Chih LeeGraduate Institute of Biomedical Sciences, China Medical University, Taichung 406040, Taiwan.ORCID 0000-0002-7718-4069
Yi-Ting ChiangDrug Development Center, China Medical University, Taichung 406040, Taiwan.ORCID 0000-0003-4614-4109
Hui-Yi LinDrug Development Center, China Medical University, Taichung 406040, Taiwan.
Der-Yen LeeGraduate Institute of Integrated Medicine, China Medical University, No. 91, Hsueh-Shih Road, Taichung 40402, Taiwan.ORCID 0000-0003-3741-8753
China Medical University · TW

Funding

China Medical University CMU108-YTY-03China Medical University CMU109-MF-102China Medical University CMU109-S-11China Medical University CMU110-S-23China Medical University CMU111-S-37Ministry of Science and Technology MOST 105-2311-B-039-003-MY2Ministry of Science and Technology MOST 107-2311-B-039-001-Ministry of Science and Technology MOST 108-2311-B-039-001-Ministry of Science and Technology MOST 109-2311-B-039-001
6 · The paper itself

Abstract

Drug combination therapy is a key approach in cancer treatments, aiming to improve therapeutic efficacy and overcome drug resistance. Evaluation of intracellular response in cancer cells to drug treatment may disclose the underlying mechanism of drug resistance. In this study, we aimed to investigate the effect of osimertinib, a tyrosine kinase inhibitor (TKI), and a curcumin derivative, 35d, on HCC827 cells and tumors by analyzing alterations in metabolome and related regulations. HCC827 tumor-bearing SCID mice and cultured HCC827 cells were separately examined. The treatment comprised four conditions: vehicle-only, 35d-only, osimertinib-only, and a combination of 35d and osimertinib. The treated tumors/cells were subsequently subjected to metabolomics profiling, fatty acyl analysis, mitochondrial potential measurement, and cell viability assay. Osimertinib induced changes in the ratio of short-chain (SC) to long-chain (LC) fatty acyls, particularly acylcarnitines (ACs), in both tumors and cells. Furthermore, 35d enhanced this effect by further lowering the SC/LC ratio of most ACs. Osimertinib and 35d also exerted detrimental effects on mitochondria through distinct mechanisms. Osimertinib upregulated the expression of carnitine palmitoyltransferase I (CPTI), while 35d induced the expression of heat shock protein 60 (HSP60). The alterations in ACs and CPTI were correlated with mitochondrial dysfunction and inhibited cell growth. Our results suggest that osimertinib and 35d disrupted the fatty acyl metabolism and induced mitochondrial stress in cancer cells. This study provides insights into the potential application of fatty acyl metabolism inhibitors, such as osimertinib or other TKIs, and mitochondrial stress inducers, such as curcumin derivatives, as combination therapy for cancer.

Indexed as

CurcuminLung NeoplasmsAcrylamidesAniline CompoundsAnimalsCell Line, TumorDrug Resistance, NeoplasmIndolesMiceMice, SCIDMitochondriaMutationProtein Kinase InhibitorsPyrimidinesAcrylamidesAniline CompoundsCurcuminIndolesosimertinibProtein Kinase InhibitorsPyrimidinesacylcarnitinecarnitinefatty acyl metabolismmetabolomicsmitochondrial stresstyrosine kinase inhibitor

Identifiers

PMID37569564
PMCPMC10418893
OpenAlexW4385422109

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.