Evidence map›Paper›PMID 35411249›Full record

ArticleAmerican journal of cancer research2022

Targeted delivery of a PROTAC induced PDEδ degrader by a biomimetic drug delivery system for enhanced cytotoxicity against pancreatic cancer cells.

Ruyu Fan, Shipeng He, Yongqing Wang, Jiaming Qiao, Hongcheng Liu, Levon Galstyan, Arman Ghazaryan, Hui Cai, Shini Feng, Pinyue Ni and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

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  8. "Biomaterials translational · 2024
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  13. Ubiquitin signaling in pancreatic ductal adenocarcinoma.Frontiers in molecular biosciences · 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

12 authors at 3 institutions in 2 countries.

Ruyu FanSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Shipeng HeInstitute of Translational Medicine, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Yongqing WangSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Jiaming QiaoSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Hongcheng LiuDepartment of Thoracic Surgery, Shanghai Pulmonary Hospital Affiliated to Tongji University Shanghai 200433, China.
Levon GalstyanSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Arman GhazaryanSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Hui CaiSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Shini FengSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Pinyue NiSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Guoqiang DongDepartment of Medicinal Chemistry, School of Pharmacy, Second Military Medical University 325 Guohe Road, Shanghai 200433, China.
Huafei LiSchool of Lifesciences, Shanghai University 333 Nanchen Road, Shanghai 200444, China.
Shanghai University · CNSecond Military Medical University · CNShanghai Pulmonary Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic carcinoma (PC) has one of the highest mortality-to-incidence ratios of any solid tumor worldwide. Although KRAS mutation is commonly found in 95% of PCs, directly targeting KRAS remains to be a highly challenging task because of its lacking catalytic pockets where molecule inhibitors can bind with. Proteolysis-targeting chimeric (PROTAC) represents an effective approach for specific degradation of disease-causing proteins by hijacking the endogenous ubiquitin-proteasome system (UPS). Previously, we designed a first-in-class PROTAC induced PDEδ degrader (PIPD), which demonstrated improved anti-tumor efficacy against KRAS mutant malignancies. However, translating cellular degradative effects from bench to beside remains a highly challenging task because of PROTAC's poor penetration efficiency across target cytomembranes and non-targeting delivery induced undesired "off target" side-effects. Herein, a smart nano-drug delivery system (CM8988-PIPD) was successfully constructed by biomimetic strategy for targeted delivery of PIPD. The biomimetic nanoparticle showed well-defined regular spherical structure with an average particle size of approximately 124.8 nm. Cancer cytomembrane camouflage endows CM8988-PIPD with excellent

Indexed as

biomimetic drug delivery systemKRAS mutationPancreatic carcinomaPDEδproteolysis-targeting chimeric

Identifiers

PMID35411249
PMCPMC8984894
OpenAlexW4225891387

What OpenQuestion 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 OpenQuestion graph.