Evidence map›Paper›PMID 35768424›Full record

ReviewSignal transduction and targeted therapy2022

Natural killer cell homing and trafficking in tissues and tumors: from biology to application.

Guang He Ran, Yu Qing Lin, Lei Tian, Tao Zhang, Dong Mei Yan, Jian Hua Yu, You Cai Deng

Open access · goldAbstract readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 192 papers.

0numbers the graph read from it
0cells of the map it votes in
192citing papers in PubMed
19.2field-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

192 citing papers in PubMed, 249 citations in OpenAlex.

  1. IL-17D reprograms CD93Cellular & molecular immunology · 2026
    Article
  2. Rbp-Jκ controls NK cell late maturation and migration via chromatin landscape remodeling.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  13. Umbilical cord blood-derived natural killer cells:Annals of medicine and surgery (2012) · 2026
    Article
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  15. Article
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132 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

7 authors at 3 institutions in 2 countries.

Guang He Ran *Department of Immunology, School of Basic Medical, Jiamusi University, 154007, Jiamusi, China.
Yu Qing Lin *Department of Immunology, School of Basic Medical, Jiamusi University, 154007, Jiamusi, China.
Lei TianDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Los Angeles, CA, 91010, USA.
Tao ZhangDepartment of Immunology, School of Basic Medical, Jiamusi University, 154007, Jiamusi, China. ztlzy1971@163.com.
Dong Mei YanDepartment of Immunology, School of Basic Medical, Jiamusi University, 154007, Jiamusi, China. yandongmei@jmsu.edu.cn.
Jian Hua YuDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Los Angeles, CA, 91010, USA. jiayu@coh.org.ORCID 0000-0002-0326-3223
You Cai DengInstitute of Materia Medica, College of Pharmacy, Army Medical University, 400038, Chongqing, China. youcai.deng@tmmu.edu.cn.ORCID 0000-0001-5488-8576
Army Medical University · CNCity Of Hope National Medical Center · USJiamusi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells, a subgroup of innate lymphoid cells, act as the first line of defense against cancer. Although some evidence shows that NK cells can develop in secondary lymphoid tissues, NK cells develop mainly in the bone marrow (BM) and egress into the blood circulation when they mature. They then migrate to and settle down in peripheral tissues, though some special subsets home back into the BM or secondary lymphoid organs. Owing to its success in allogeneic adoptive transfer for cancer treatment and its "off-the-shelf" potential, NK cell-based immunotherapy is attracting increasing attention in the treatment of various cancers. However, insufficient infiltration of adoptively transferred NK cells limits clinical utility, especially for solid tumors. Expansion of NK cells or engineered chimeric antigen receptor (CAR) NK cells ex vivo prior to adoptive transfer by using various cytokines alters the profiles of chemokine receptors, which affects the infiltration of transferred NK cells into tumor tissue. Several factors control NK cell trafficking and homing, including cell-intrinsic factors (e.g., transcriptional factors), cell-extrinsic factors (e.g., integrins, selectins, chemokines and their corresponding receptors, signals induced by cytokines, sphingosine-1-phosphate (S1P), etc.), and the cellular microenvironment. Here, we summarize the profiles and mechanisms of NK cell homing and trafficking at steady state and during tumor development, aiming to improve NK cell-based cancer immunotherapy.

Indexed as

Immunity, InnateNeoplasmsBiologyCytokinesHumansKiller Cells, NaturalTumor MicroenvironmentCytokines

Identifiers

PMID35768424
PMCPMC9243142
OpenAlexW4283752716

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.