Evidence map›Paper›PMID 35286780›Full record

ArticleAdvanced healthcare materials2022

Vascularized Lung Cancer Model for Evaluating the Promoted Transport of Anticancer Drugs and Immune Cells in an Engineered Tumor Microenvironment.

Dasom Kim, Kyeong Seob Hwang, Eun U Seo, Suyeong Seo, Byung Chul Lee, Nakwon Choi, Jonghoon Choi, Hong Nam Kim

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  9. Advances and challenges in human 3D solid tumor models.Advanced functional materials · 2025
    Article
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  19. Tumor-on-chip platforms for breast cancer continuum concept modeling.Frontiers in bioengineering and biotechnology · 2024
    Review
  20. Microphysiological systems as models for immunologically 'cold' tumors.Frontiers in cell and developmental biology · 2024
    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

8 authors at 5 institutions in 1 country.

Dasom KimBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Kyeong Seob HwangBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Eun U SeoBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Suyeong SeoBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Byung Chul LeeBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Nakwon ChoiBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Jonghoon ChoiSchool of Integrative Engineering, Chung-Ang University, Seoul, 06974, Republic of Korea.
Hong Nam KimBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.ORCID 0000-0002-0329-0029
Korea Institute of Brain Science · KRYonsei University · KRChung-Ang University · KRKorea University · KRSeoul National University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment (TME) is the environment around the tumor, including blood vessels, immune cells, fibroblasts, signaling molecules, and the extracellular matrix (ECM). Owing to its component interactions, the TME influences tumor growth and drug delivery in a highly complex manner. Although several vascularized cancer models are developed to mimic the TME in vitro, these models cannot comprehensively reflect blood vessel-tumor spheroid interactions. Here, a method for inducing controlled tumor angiogenesis by engineering the microenvironment is presented. The interstitial flow direction regulates the direction of capillary sprouting, showing that angiogenesis occurs in the opposite direction of flow, while the existence of lung fibroblasts affects the continuity and lumen formation of sprouted capillaries. The vascularized tumor model shows enhanced delivery of anticancer drugs and immune cells to the tumor spheroids because of the perfusable vascular networks. The possibility of capillary embolism using anticancer drug-conjugated liquid metal nanoparticles is investigated using the vascularized tumor model. This vascularized tumor platform can aid in the development of effective anticancer drugs and cancer immunotherapy.

Indexed as

Antineoplastic AgentsLung NeoplasmsHumansLungNeovascularization, PathologicTumor MicroenvironmentAntineoplastic Agentsangiogenesisdrug deliveryimmune cell transporttumor spheroidsvascularization

Identifiers

PMID35286780
PMCPMC11468795
OpenAlexW4221025264

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.