Evidence map›Paper›PMID 37424037›Full record

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

A PDA-Functionalized 3D Lung Scaffold Bioplatform to Construct Complicated Breast Tumor Microenvironment for Anticancer Drug Screening and Immunotherapy.

Wanheng Zhang, Yan Chen, Mengyuan Li, Shucheng Cao, Nana Wang, Yingjian Zhang, Yongtao Wang

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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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 5 institutions in 2 countries.

Wanheng ZhangDepartment of Pharmacy, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471003, China.
Yan ChenDepartment of Pharmacy, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471003, China.
Mengyuan LiSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Shucheng CaoDepartment of Quantitative Life Sciences, McGill University, Montréal, Québec, H3A 0G4, Canada.
Nana WangDepartment of Pediatrics, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, 200080, China.
Yingjian ZhangDepartment of Pharmacy, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471003, China.
Yongtao WangShanghai Engineering Research Center of Organ Repair, School of Medicine, Shanghai University, Shanghai, 200444, China.ORCID 0000-0001-5148-9393
First Affiliated Hospital of Henan University of Science and Technology · CNMcGill University · CANanjing University of Chinese Medicine · CNShanghai Jiao Tong University · CNShanghai University · CN

Funding

Natural Science Foundation in Shanghai General Hospital 02Natural Science Foundation in Shanghai General Hospital 06Natural Science Foundation in Shanghai General Hospital 22Natural Science Foundation in Shanghai General Hospital 72Shanghai Overseas High-Level Talent 213Shanghai Overseas High-Level Talent 23Shanghai Overseas High-Level Talent 58Shanghai Overseas High-Level Talent D305
6 · The paper itself

Abstract

2D cell culture occupies an important place in cancer progression and drug discovery research. However, it limitedly models the "true biology" of tumors in vivo. 3D tumor culture systems can better mimic tumor characteristics for anticancer drug discovery but still maintain great challenges. Herein, polydopamine (PDA)-modified decellularized lung scaffolds are designed and can serve as a functional biosystem to study tumor progression and anticancer drug screening, as well as mimic the tumor microenvironment. PDA-modified scaffolds with strong hydrophilicity and excellent cell compatibility can promote cell growth and proliferation. After 96 h treatment with 5-FU, cisplatin, and DOX, higher survival rates in PDA-modified scaffolds are observed compared to nonmodified scaffolds and 2D systems. The E-cadhesion formation, HIF-1α-mediated senescence decrease, and tumor stemness enhancement can drive drug resistance and antitumor drug screening of breast cancer cells. Moreover, there is a higher survival rate of CD45

Indexed as

Antineoplastic AgentsNeoplasmsCD8-Positive T-LymphocytesHumansImmunotherapyIndolesLungPolymersTissue ScaffoldsTumor MicroenvironmentAntineoplastic AgentsIndolespolydopaminePolymersbreast cancer cellsdrug resistance screeningPDA-modified lung scaffoldstumor immunotherapyunderlying mechanism

Identifiers

PMID37424037
PMCPMC10502821
OpenAlexW4383711210

What OpenQuestion holds

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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.