Evidence map›Paper›PMID 37485650›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Micro-Engineered Organoid-on-a-Chip Based on Mesenchymal Stromal Cells to Predict Immunotherapy Responses of HCC Patients.

Zhengyu Zou, Zhun Lin, Chenglin Wu, Jizhou Tan, Jie Zhang, Yanwen Peng, Kunsong Zhang, Jiaping Li, Minhao Wu, Yuanqing Zhang

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 76 citations in OpenAlex.

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8 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Zhengyu ZouZhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.ORCID 0000-0002-8425-0220
Zhun LinSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Chenglin WuThe First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Jizhou TanThe First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Jie ZhangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Yanwen PengThe Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510635, China.
Kunsong ZhangThe First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Jiaping LiThe First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Minhao WuZhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.ORCID 0000-0002-8711-868X
Yuanqing ZhangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.ORCID 0000-0002-8761-5328
Sun Yat-sen University · CN

Funding

111 Project B12003111 Project B13037China Postdoctoral Science Foundation 2022M723661Fundamental Research Funds for the Central Universities 19ykzd39National Natural Science Foundation of China 31970893National Natural Science Foundation of China 32270976National Natural Science Foundation of China 82072087Natural Science Foundation of Guangdong Province 2022A1515012541Natural Science Foundation of Guangdong Province 2023A1515030062Science and Technology Projects in Guangzhou 202206010087
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most lethal cancers worldwide. Patient-derived organoid (PDO) has great potential in precision oncology, but low success rate, time-consuming culture, and lack of tumor microenvironment (TME) limit its application. Mesenchymal stromal cells (MSC) accumulate in primary site to support tumor growth and recruit immune cells to form TME. Here, MSC and peripheral blood mononuclear cells (PBMC) coculture is used to construct HCC organoid-on-a-chip mimicking original TME and provide a high-throughput drug-screening platform to predict outcomes of anti-HCC immunotherapies. HCC-PDOs and PBMC are co-cultured with MSC and Cancer-associated fibroblasts (CAF). MSC increases success rate of biopsy-derived PDO culture, accelerates PDO growth, and promotes monocyte survival and differentiation into tumor-associated macrophages. A multi-layer microfluidic chip is designed to achieve high-throughput co-culture for drug screening. Compared to conventional PDOs, MSC-PDO-PBMC and CAF-PDO-PBMC models show comparable responses to chemotherapeutic or targeted anti-tumor drugs but more precise prediction potential in assessing patients' responses to anti-PD-L1 drugs. Moreover, this microfluidic platform shortens PDO growth time and improves dimensional uniformity of organoids. In conclusion, the study successfully constructs microengineered organoid-on-a-chip to mimic TME for high-throughput drug screening, providing novel platform to predict immunotherapy response of HCC patients.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMesenchymal Stem CellsHumansImmunotherapyLab-On-A-Chip DevicesLeukocytes, MononuclearOrganoidsPrecision MedicineTumor Microenvironmentcancer immunotherapydrug screeningmesenchymal stromal cellsmicrofluidicstumor organoids

Identifiers

PMID37485650
PMCPMC10520686
OpenAlexW4385186958

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.