Evidence map›Paper›PMID 38338418›Full record

ArticleMolecules (Basel, Switzerland)2024

Co-Delivery of Gemcitabine and Honokiol by Lipid Bilayer-Coated Mesoporous Silica Nanoparticles Enhances Pancreatic Cancer Therapy via Targeting Depletion of Tumor Stroma.

Dan Liu, Linjiang Wang, Henan Li, Dong Li, Jianwen Zhou, Jing Wang, Qi Zhang, Defu Cai

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.5field-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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Clinical application and drug resistance mechanism of gemcitabine.Frontiers in cell and developmental biology · 2025
    Review
  5. Review
  6. 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

8 authors at 1 institution in 1 country.

Dan LiuInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Linjiang WangInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Henan LiInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Dong LiInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Jianwen ZhouInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Jing WangInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Qi ZhangInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.
Defu CaiInstitute of Medicine and Drug Research, Qiqihar Medical University, Qiqihar 161006, China.ORCID 0000-0001-7673-7859
Qiqihar Medical University · CN

Funding

Heilongjiang Provincial Natural Science Foundation of China JQ2020H004National Natural Science Foundation of China 81873172Qiqihar Science and Technology Bureau LHYD-2021008Scientific Research Fund of Heilongjiang Provincial Education Department, China 2021-KYYWF-0365, 2019-KYYWF-1275Scientific Research Fund of Qiqihar Academy of Medical Sciences, China QMSI2022Z-12, 2021-ZDPY-013
6 · The paper itself

Abstract

Syndecan-1 (SDC1) modified lipid bilayer (LB)-coated mesoporous silica nanoparticles (MSN) to co-deliver gemcitabine (GEM) and honokiol (HNK) were prepared for the targeting treatment of pancreatic cancer. The encapsulation efficiencies of GEM and HNK in SDC1-LB-MSN-GEM/HNK were determined to be 60.3 ± 3.2% and 73.0 ± 1.1%. The targeting efficiency of SDC1-LB-MSN-GEM/HNK was investigated in BxPC-3 cells in vitro. The fluorescence intensity in the cells treated with SDC1-LB-MSN-Cou6 was 2-fold of LB-MSN-Cou6-treated cells, which was caused by SDC1/IGF1R-mediated endocytosis. As anticipated, its cytotoxicity was significantly increased. Furthermore, the mechanism was verified that SDC1-LB-MSN-HNK induced tumor cell apoptosis through the mitochondrial apoptosis pathway. Finally, the biodistribution, tumor growth inhibition, and preliminary safety studies were performed on BALB/c nude mice bearing BxPC-3 tumor models. The tumor growth inhibition index of SDC1-LB-MSN-GEM/HNK was 56.19%, which was 1.45-fold and 1.33-fold higher than that of the free GEM/HNK and LB-MSN-GEM/HNK treatment groups, respectively. As a result, SDC1-LB-MSN-GEM/HNK combined advantages of both GEM and HNK and simultaneously targeted and eliminated pancreatic cancerous and cancer-associated stromal cells. In summary, the present study demonstrated a new strategy of synergistic GEM and HNK to enhance the therapeutic effect of pancreatic cancer via the targeting depletion of tumor stroma.

Indexed as

Allyl CompoundsBiphenyl CompoundsNanoparticlesPancreatic NeoplasmsPhenolsAnimalsCell Line, TumorGemcitabineLipid BilayersMiceMice, NudeSilicon DioxideTissue DistributionAllyl CompoundsBiphenyl CompoundsGemcitabinehonokiolLipid BilayersPhenolsSilicon Dioxidegemcitabinehonokiollipid bilayer-coated mesoporous silica nanoparticlessyndecan-1targeting tumor stroma

Identifiers

PMID38338418
PMCPMC10856273
OpenAlexW4391433283

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.