Evidence map›Paper›PMID 34758094›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2022

Advanced Nanoengineering Approach for Target-Specific, Spatiotemporal, and Ratiometric Delivery of Gemcitabine-Cisplatin Combination for Improved Therapeutic Outcome in Pancreatic Cancer.

Mubin Tarannum, Md Akram Hossain, Bryce Holmes, Shan Yan, Pinku Mukherjee, Juan L Vivero-Escoto

Open access · greenAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  14. Article
  15. Platinum-based combination nanomedicines for cancer therapy.Current opinion in chemical biology · 2023
    Review
  16. Article
  17. Article
  18. Advances and Prospects in the Treatment of Pancreatic Cancer.International journal of nanomedicine · 2023
    Review
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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

6 authors at 2 institutions in 1 country.

Mubin TarannumDepartment of Chemistry, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.
Md Akram HossainDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.
Bryce HolmesAnalytical Research Laboratory, North Carolina A&T State University, Greensboro, NC, 27411, USA.
Shan YanDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.
Pinku MukherjeeDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.
Juan L Vivero-EscotoDepartment of Chemistry, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.ORCID 0000-0001-7400-2963
University of North Carolina at Charlotte · USNorth Carolina Agricultural and Technical State University · US

Funding

Stimuli-responsive mucin1-specific nanoparticles for efficacious combinatorial chemotherapy of pancreatic ductal adenocarcinomaR01CA263897 · NCI · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI Juan Luis Vivero-Escoto · 2022 to 2026
$2.0M
Mechanism of APE1 in DNA damage responseR01CA225637 · NCI · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI YAN, SHAN · 2018 to 2022
$1.9M
Multifunctional nanoparticles for combinational therapy of pancreatic cancerR15CA192160 · NCI · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI VIVERO-ESCOTO, JUAN LUIS · 2015 to 2015
$437k
NCI NIH HHS R01 CA225637NCI NIH HHS R01 CA263897NCI NIH HHS R15 CA192160
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is an intractable malignancy with a dismal survival rate. Recent combination therapies have had a major impact on the improvement of PDAC prognosis. Nevertheless, clinically used combination regimens such as FOLFIRINOX and gemcitabine (Gem)/nab-paclitaxel still face major challenges due to lack of the safe and ratiometric delivery of multiple drugs. Here, a rationally designed mesoporous silica nanoparticle (MSN)-based platform is reported for the target-specific, spatiotemporal, ratiometric, and safe co-delivery of Gem and cisplatin (cisPt). It is shown that systemic administration of the nanoparticles results in synergistic therapeutic outcome in a syngeneic and clinically relevant genetically engineered PDAC mouse model that has rarely been used for the therapeutic evaluation of nanomedicine. This synergism is associated with a strategic engineering approach, in which nanoparticles provide redox-responsive controlled delivery and in situ differential release of Gem/cisPt drugs with the goal of overcoming resistance to Pt-based drugs. The platform is also rendered with additional tumor-specificity via a novel tumor-associated mucin1 (tMUC1)-specific antibody, TAB004. Overall, the platform suppresses tumor growth and eliminates the off-target toxicities of a highly toxic chemotherapy combination.

Indexed as

Pancreatic NeoplasmsAlbuminsAnimalsAntineoplastic Combined Chemotherapy ProtocolsCisplatinDeoxycytidineGemcitabineMicePaclitaxelTreatment OutcomeAlbuminsCisplatinDeoxycytidineGemcitabinePaclitaxelcombinatorial therapypancreatic cancerspatiotemporal releasetargeted drug delivery

Identifiers

PMID34758094
PMCPMC8758547
OpenAlexW3212579124

What OpenQuestion 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 OpenQuestion graph.