Evidence map›Paper›PMID 42402596›Full record

ReviewMicrosystems & nanoengineering2026

From single cell analysis to 3D micro physiological systems: microfluidic tools integrating cancer cell targets for delineating natural killer cell biology.

Maria V Hangad, Heqing Ma, Sam K P Kung, Francis Lin

Abstract readReview
In one paragraph

Review in Microsystems & nanoengineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Maria V HangadDepartment of Immunology, University of Manitoba, Winnipeg, MB, Canada.
Heqing MaDepartment of Immunology, University of Manitoba, Winnipeg, MB, Canada.
Sam K P KungDepartment of Immunology, University of Manitoba, Winnipeg, MB, Canada. sam.kung@umanitoba.ca.
Francis LinDepartment of Immunology, University of Manitoba, Winnipeg, MB, Canada. francis.lin@umanitoba.ca.

Funding

Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada) RGPIN-2021-03346Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada) RGPIN/4504-2022
6 · The paper itself

Abstract

Natural killer cell is a critical cell type in our immune system. Its therapeutic potential in the development of novel cancer immunotherapy has been emerging. Microfluidic technologies capable of manipulating small volumes of fluid through microchannels are emerging tools for advancing our knowledge of natural killer cell biology. However, the rationale behind microfluidic device design, material choice, and the precise engineering of in vitro microenvironments has yet to be systematically assessed through the lens of complex NK cell biology using cancer cells as targets for activation. This comprehensive review assesses microfluidic technologies designed for the study of NK cell phenotype/function at a single cell level, migration dynamics in the presence or absence of biochemical cues, natural killer-target cell interactions, and observation of sophisticated cellular behavior (infiltration/cytotoxicity) in multi-factorial complex microenvironments. Step by step advances in device complexity such as the integration of acellular hydrogels or multicellular co-culture systems highlight the emerging need for higher resolution analysis of natural killer cell properties at the single cell, tissue, and organ levels. The progression of microfluidic technologies for advancing knowledge of natural killer (NK) cell biological mechanisms within the last twenty years. Figure was generated using BioRender.

Identifiers

PMID42402596
PMCPMC13333826

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.