Evidence map›Paper›PMID 39817244›Full record

ArticleAnnals of translational medicine2024

Cell type-specific upregulation of NKG2D ligand MICA in response to APTO253.

Reem Alkhayer, Viviane Ponath, Elke Pogge von Strandmann

Abstract read
In one paragraph

Article in Annals of translational medicine, 2024. 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

3 authors.

Reem Alkhayer *Institute for Tumor Immunology, Center for Tumor Biology and Immunology, Philipps-University Marburg, Marburg, Germany.
Viviane Ponath *Institute for Tumor Immunology, Center for Tumor Biology and Immunology, Philipps-University Marburg, Marburg, Germany.
Elke Pogge von StrandmannInstitute for Tumor Immunology, Center for Tumor Biology and Immunology, Philipps-University Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0003-4785-9165

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the most important targets for natural killer (NK) cell-mediated therapy is the induction of natural killer group 2D ligand (NKG2D-L) expression. APTO253 is a small molecule that selectively kills acute myeloid leukemia (AML) cells, and it has been reported that APTO253 can induce Krüppel-like factor 4 (KLF4) expression and downregulate c-MYC expression. Recently, we discovered a novel role of APTO253 in modulating the NK cell response by inducing surface expression of NKG2D-Ls, especially MHC class I polypeptide-related sequence A (MICA), in AML cells. In this study, we extended the research to validate the effect of APTO253 in other cancer cell lines and found that the enhanced expression of NKG2D-Ls in response to APTO253 is limited in a tumor cell-specific manner. Here, we show that MICA induction upon treatment with APTO253 not only varies between ovarian and pancreatic cancer cell lines but also differs in two ovarian cancer cell lines for an unknown reason. Additionally, our data suggest a link between the induced expression of

Indexed as

APTO253MHC class I polypeptide-related sequence A induction (MICA induction)natural killer cell-mediated therapy (NK cell-mediated therapy)natural killer group 2D (NKG2D)

Identifiers

PMID39817244
PMCPMC11729809

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Registered trials

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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.