Evidence map›Paper›PMID 37772330›Full record

ArticleJournal of biomedical materials research. Part A2024

TRAIL-conjugated liposomes that bind natural killer cells to induce colorectal cancer cell apoptosis.

Joshua D Greenlee, Zhenjiang Zhang, Tejas Subramanian, Kevin Liu, Michael R King

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. 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

5 authors at 1 institution in 1 country.

Joshua D GreenleeDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
Zhenjiang ZhangDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
Tejas SubramanianDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
Kevin LiuDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
Michael R KingDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID 0000-0002-0223-7808
Vanderbilt University · US

Funding

Super Natural Killer Cells That Target Metastases in the Tumor-Draining Lymph NodesR01CA203991 · NCI · VANDERBILT UNIVERSITY · PI KING, MICHAEL R. · 2017 to 2021
$1.9M
Enabling Technology to Study Mechanosensitive and Mechanoresistant Cancer Cells in FlowR01CA256054 · NCI · VANDERBILT UNIVERSITY · PI KING, MICHAEL R. · 2021 to 2025
$1.8M
NCI NIH HHS R01 CA203991NCI NIH HHS R01 CA256054NIH HHS R01CA203991NIH HHS R01CA256054
6 · The paper itself

Abstract

Natural killer (NK) cell functionality is a strong indicator of favorable prognosis in cancer patients, making NK cells an appealing therapeutic target to prevent lymph node dissemination. We engineered liposomes that are conjugated with anti-CD335 antibodies for NK cell targeting, and the apoptotic ligand TRAIL to kill cancer cells. Liposomes were made using a thin film hydration method followed by extrusion to approximately 100 nm in diameter and conjugation of proteins via thiol-maleimide click chemistry. TRAIL/anti-CD335 liposomes successfully bound to isolated NK cells. Once piggybacked to the surface of NK cells, these "Super Natural Killer Cells" were able to more effectively kill oxaliplatin-resistant SW620 cells and metastatic COLO205 colorectal cancer cells via TRAIL-mediated apoptosis compared to NK cells alone. Importantly, Super NK cells were more effective under physiological levels of fluid shear stress found in the lymphatics. Liposome biodistribution after intravenous administration confirmed the sustained presence of liposomes within the spleen and tumor draining mesenteric lymph nodes for at least 4 days. These results demonstrate the enhanced apoptotic effects of NK cells armored with liposomal TRAIL against clinically relevant colorectal cancer cells, providing the groundwork for in vivo treatment studies in mouse models of colorectal cancer metastasis.

Indexed as

Colonic NeoplasmsLiposomesAnimalsApoptosisCytotoxicity, ImmunologicHumansKiller Cells, NaturalMiceTissue DistributionLiposomesliposomeslymphaticsnatural killer cellsTRAIL

Identifiers

PMID37772330
PMCPMC10794038
OpenAlexW4387157897

What Socratic holds

Textmetadata
LicenceTDM
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.