Evidence map›Paper›PMID 36739414›Full record

ArticleJournal of nanobiotechnology2023

Acoustofluidic assembly of primary tumor-derived organotypic cell clusters for rapid evaluation of cancer immunotherapy.

Zhuhao Wu, Zheng Ao, Hongwei Cai, Xiang Li, Bin Chen, Honglei Tu, Yijie Wang, Rongze Olivia Lu, Mingxia Gu, Liang Cheng and 2 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Human brain organoids for understanding substance use disorders.Drug metabolism and pharmacokinetics · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Engineering Heterogeneous Tumor Models for Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  13. Acoustofluidic Engineering of Functional Vessel-on-a-Chip.ACS biomaterials science & engineering · 2023
    Article
  14. Article
  15. Article
  16. 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

12 authors.

Zhuhao WuDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA.
Zheng AoDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA. aozheng.89@gmail.com.
Hongwei CaiDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA.
Xiang LiDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA.
Bin ChenDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA.
Honglei TuDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA.
Yijie WangComputer Science Department, Indiana University, Bloomington, IN, 47408, USA.
Rongze Olivia LuDepartment of Neurological Surgery, Brain Tumor Center, Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, California, CA, 94143, USA.
Mingxia GuCenter for Stem Cell and Organoid Medicine (CuSTOM), Division of Pulmonary Biology, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Liang ChengDepartment of Pathology and Laboratory Medicine, Brown University Warren Alpert Medical School, Lifespan Academic Medical Center, and the Legorreta Cancer Center at Brown University, Providence, RI, 02903, USA.
Xin LuDepartment of Biological Sciences, Boler-Parseghian Center for Rare and Neglected Diseases, Harper Cancer Research Institute, University of Notre Dame, Notre Dame, IN, 46556, USA.
Feng GuoDepartment of Intelligent Systems Engineering, Indiana University, Bloomington, IN, 47405, USA. fengguo@iu.edu.

Funding

Unfolded Protein Response and Autophagy in T Helper Cell Effector FunctionP20GM121176 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Praveen K Balne · 2017 to 2026
$24.9M
An automated portable system for detecting and treating opioid induced respiratory depressionU01DA056242 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI GUO, FENG, MACKIE, KENNETH · 2022 to 2024
$3.8M
Early detection of type 1 diabetes via Exosome Technology with Optoelectronics Lab-on-chip: EXTOLR01DK133864 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI GAGLIA, JASON, GUO, FENG · 2022 to 2025
$3.0M
An acoustofluidic avidity cytometer for massive parallel profiling single autoreactive T cell in autoimmune diseaseDP2AI160242 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI GUO, FENG · 2020 to 2020
$2.4M
Acquisition of a DeltaVision OMX-SR Imaging SystemS10OD024988 · OD · INDIANA UNIVERSITY INDIANAPOLIS · PI WALCZAK, CLAIRE E · 2018 to 2018
$600k
Acoustic assembly of patient tumor organoids for modeling cancer immunityR03EB030331 · NIBIB · TRUSTEES OF INDIANA UNIVERSITY · PI GUO, FENG · 2020 to 2021
$159k
NIAID NIH HHS DP2 AI160242NIBIB NIH HHS R03 EB030331NIDA NIH HHS U01 DA056242NIDDK NIH HHS R01 DK133864NIGMS NIH HHS P20 GM121176NIH HHS S10 OD024988
6 · The paper itself

Abstract

Cancer immunotherapy shows promising potential for treating breast cancer. While patients may have heterogeneous treatment responses for adjuvant therapy, it is challenging to predict an individual patient's response to cancer immunotherapy. Here, we report primary tumor-derived organotypic cell clusters (POCCs) for rapid and reliable evaluation of cancer immunotherapy. By using a label-free, contactless, and highly biocompatible acoustofluidic method, hundreds of cell clusters could be assembled from patient primary breast tumor dissociation within 2 min. Through the incorporation of time-lapse living cell imaging, the POCCs could faithfully recapitulate the cancer-immune interaction dynamics as well as their response to checkpoint inhibitors. Superior to current tumor organoids that usually take more than two weeks to develop, the POCCs can be established and used for evaluation of cancer immunotherapy within 12 h. The POCCs can preserve the cell components from the primary tumor due to the short culture time. Moreover, the POCCs can be assembled with uniform fabricate size and cell composition and served as an open platform for manipulating cell composition and ratio under controlled treatment conditions with a short turnaround time. Thus, we provide a new method to identify potentially immunogenic breast tumors and test immunotherapy, promoting personalized cancer therapy.

Indexed as

Breast NeoplasmsFemaleHumansImmunotherapyAcoustofluidicsCancer immunotherapyCancer modelsCell clustersMicrofluidics

Identifiers

PMID36739414
PMCPMC9899402

What Socratic 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 Socratic graph.