Evidence map›Paper›PMID 41923319›Full record

ArticleCancer science2026

SLPI/FBW7/c-Myc Axis Reduces Gemcitabine Sensitivity in PDAC by Enhancing Glycolysis and Impairing NK Cell Immunity.

Haofei Chen, Xin Li, Weixiong Zhu, Yanxi Mu, Guoqing Zhang, Youheng Zhang, Yusheng Cheng, Wence Zhou

Abstract read
In one paragraph

Article in Cancer science, 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

8 authors.

Haofei ChenThe Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.ORCID https://orcid.org/0000-0002-4134-5326
Xin LiDepartment of General Surgery, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.
Weixiong ZhuThe Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.
Yanxi MuThe Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.
Guoqing ZhangThe Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.
Youheng ZhangThe Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.
Yusheng ChengDepartment of General Surgery, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.
Wence ZhouThe Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, China.ORCID https://orcid.org/0000-0002-0529-7777

Funding

Cuiying Science and Technology Innovation Project of the Second Hospital of Lanzhou University CY2024-CQ-01National Natural Science Foundation of China 82260555
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive malignancy with dismal prognosis. Although gemcitabine works by directly inducing tumor cell death, as well as activating NK cell-mediated antitumor immunity, its efficacy remains rather unsatisfying. Currently, biomarkers precisely ascertaining gemcitabine resistance in PDAC are unavailable; thus, it is of much urgency to identify biomarkers accurately predicting gemcitabine sensitivity and explore innovative targets for developing sensitization strategy. Secretory leukocyte protease inhibitor (SLPI) is overexpressed in several solid tumors, but its role in PDAC remains unclear. This study aims to elucidate the function and mechanism of SLPI in modulating gemcitabine sensitivity in PDAC. In this study, we found that SLPI was markedly upregulated in PDAC cell lines and tissues, inversely correlating with gemcitabine efficacy and survival outcome of patients. In vitro, SLPI overexpression significantly reduced PDAC cell sensitivity to gemcitabine-induced direct cytotoxicity and NK cell-mediated lysis through enhancing c-Myc-driven glycolysis, whereas SLPI knockdown generated the opposite effects. Mechanistically, SLPI could directly interact with c-Myc protein, which disturbed the binding of E3 ubiquitin ligase FBW7 to c-Myc and thereby prevented ubiquitination-mediated c-Myc degradation, resultantly increasing c-Myc stability and expression. In vivo, SLPI knockdown substantially sensitized gemcitabine treatment to suppress PDAC growth, and this effect was at least partly dependent on NK cell-mediated antitumor immunity. Totally, our findings support that SLPI may serve as a promising biomarker for predicting gemcitabine therapy response, and targeting SLPI may be an effective strategy to improve gemcitabine efficacy in PDAC patients. All procedures involving animals were conducted in compliance with institutional ethics regulations and approved by the Ethics Committee of the Second Hospital of Lanzhou University (Approval No. D2025-434).

Indexed as

Carcinoma, Pancreatic DuctalDeoxycytidineKiller Cells, NaturalPancreatic NeoplasmsProto-Oncogene Proteins c-mycSecretory Leukocyte Peptidase InhibitorAnimalsAntimetabolites, AntineoplasticCell Line, TumorDrug Resistance, NeoplasmF-Box ProteinsFemaleGemcitabineGene Expression Regulation, NeoplasticGlycolysisHumansAntimetabolites, AntineoplasticDeoxycytidineF-Box ProteinsGemcitabineMYC protein, humanProto-Oncogene Proteins c-mycSecretory Leukocyte Peptidase InhibitorSLPI protein, humangemcitabineglycolysisNK cellsPDACSLPI

Identifiers

PMID41923319
PMCPMC13580765

What Socratic holds

Textmetadata
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.