Evidence map›Paper›PMID 34262860›Full record

ArticleFrontiers in oncology2021

Tumor Microenvironment Alters Chemoresistance of Hepatocellular Carcinoma Through CYP3A4 Metabolic Activity.

Alican Özkan, Danielle L Stolley, Erik N K Cressman, Matthew McMillin, Sharon DeMorrow, Thomas E Yankeelov, Marissa Nichole Rylander

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 47 citations in OpenAlex.

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  17. Down-Regulation of CYP3A4 by the KInternational journal of molecular sciences · 2023
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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

7 authors at 4 institutions in 1 country.

Alican ÖzkanDepartment of Mechanical Engineering, The University of Texas, Austin, TX, United States.
Danielle L StolleyDepartment of Biomedical Engineering, The University of Texas, Austin, TX, United States.
Erik N K CressmanDepartment of Interventional Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Matthew McMillinDepartment of Internal Medicine, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Sharon DeMorrowDepartment of Internal Medicine, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Thomas E YankeelovDepartment of Biomedical Engineering, The University of Texas, Austin, TX, United States.
Marissa Nichole RylanderDepartment of Mechanical Engineering, The University of Texas, Austin, TX, United States.
The University of Texas at Austin · USCentral Texas Veterans Health Care System · USLivestrong Foundation · USThe University of Texas MD Anderson Cancer Center · US

Funding

Simultaneous Thermal and Osmotic Stresses in Tumor Ablation: Imaging and BiologyR01CA201127 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CRESSMAN, ERIK N · 2016 to 2020
$2.3M
Pathogenic role of thrombospondin-1 in acute and chronic liver failureIK2BX003486 · VA · OLIN TEAGUE VETERANS CENTER · PI MCMILLIN, MATTHEW · 2017 to 2022
–
BLRD VA IK2 BX003486NCI NIH HHS R01 CA201127
6 · The paper itself

Abstract

Variations in tumor biology from patient to patient combined with the low overall survival rate of hepatocellular carcinoma (HCC) present significant clinical challenges. During the progression of chronic liver diseases from inflammation to the development of HCC, microenvironmental properties, including tissue stiffness and oxygen concentration, change over time. This can potentially impact drug metabolism and subsequent therapy response to commonly utilized therapeutics, such as doxorubicin, multi-kinase inhibitors (e.g., sorafenib), and other drugs, including immunotherapies. In this study, we utilized four common HCC cell lines embedded in 3D collagen type-I gels of varying stiffnesses to mimic normal and cirrhotic livers with environmental oxygen regulation to quantify the impact of these microenvironmental factors on HCC chemoresistance. In general, we found that HCC cells with higher baseline levels of cytochrome p450-3A4 (CYP3A4) enzyme expression, HepG2 and C3Asub28, exhibited a cirrhosis-dependent increase in doxorubicin chemoresistance. Under the same conditions, HCC cell lines with lower CYP3A4 expression, HuH-7 and Hep3B2, showed a decrease in doxorubicin chemoresistance in response to an increase in microenvironmental stiffness. This differential therapeutic response was correlated with the regulation of CYP3A4 expression levels under the influence of stiffness and oxygen variation. In all tested HCC cell lines, the addition of sorafenib lowered the required doxorubicin dose to induce significant levels of cell death, demonstrating its potential to help reduce systemic doxorubicin toxicity when used in combination. These results suggest that patient-specific tumor microenvironmental factors, including tissue stiffness, hypoxia, and CYP3A4 activity levels, may need to be considered for more effective use of chemotherapeutics in HCC patients.

Indexed as

3D cell culturechemoresistancecirrhosisdesmoplasiadrug metabolizationhepatocellular carcinomahypoxiatissue engineering

Identifiers

PMID34262860
PMCPMC8273608
OpenAlexW3175278429

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.