Evidence map›Paper›PMID 33975498›Full record

ArticleDrug delivery2021

Synergistic effect of the anti-PD-1 antibody with blood stable and reduction sensitive curcumin micelles on colon cancer.

Feirong Gong, Jian-Chao Ma, Jianguo Jia, Fa-Zhan Li, Jiao-Lan Wu, Shanfeng Wang, Xin Teng, Zhong-Kai Cui

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Feirong GongKey Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, China.
Jian-Chao MaDepartment of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0002-7739-5819
Jianguo JiaDepartment of Cardiology, Shanghai Institute of Cardiovascular Disease, Zhongshan Hospital, Fudan University, Shanghai, China.
Fa-Zhan LiDepartment of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0002-6589-2033
Jiao-Lan WuDepartment of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0002-3066-9261
Shanfeng WangSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Xin TengKey Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, China.ORCID https://orcid.org/0000-0001-5712-3202
Zhong-Kai CuiDepartment of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0003-3112-9379
East China University of Science and Technology · CNSouthern Medical University · CNSun Yat-sen University · CNThird Affiliated Hospital of Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Curcumin (1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) is a potent anticancer drug with versatile biological activities, while the clinical translation of curcumin is severely limited due to its hydrophobicity, rapid elimination, and metabolism in the blood circulation. Herein, we aim to unravel the potential of curcumin as a synergistic agent with immunotherapy in the treatment of cancers. In an effort to minimize premature release and improve the systemic bioavailability, a superior blood stable and reduction sensitive curcumin micellar formulation, of which the release can be triggered by cancer cells, is rationally designed. We have synthesized a telodendrimer (mPEG-PLA-(LA)

Indexed as

MicellesAnimalsAntineoplastic AgentsAntineoplastic Agents, ImmunologicalCell LineCell Line, TumorChemistry, PharmaceuticalColonic NeoplasmsCurcuminDelayed-Action PreparationsDrug CarriersDrug LiberationDrug StabilityDrug SynergismFemaleHemolysisAntineoplastic AgentsAntineoplastic Agents, ImmunologicalCurcuminDelayed-Action PreparationsDrug CarriersMicellesProgrammed Cell Death 1 Receptorbioavailabilitycancer immunotherapyglutathione-triggered releasesynergistic effectTelodendrimer micelles

Identifiers

PMID33975498
PMCPMC8118404
OpenAlexW3161355401

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.