Evidence map›Paper›PMID 26365295›Full record

ArticleAngewandte Chemie (International ed. in English)2015

Enzyme-Instructed Intracellular Molecular Self-Assembly to Boost Activity of Cisplatin against Drug-Resistant Ovarian Cancer Cells.

Jie Li, Yi Kuang, Junfeng Shi, Jie Zhou, Jamie E Medina, Rong Zhou, Dan Yuan, Cuihong Yang, Huaimin Wang, Zhimou Yang and 3 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

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  13. Supramolecular Nanomedicines ofFrontiers in chemistry · 2022
    Review
  14. Article
  15. Article
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  17. Metal-Coordinated Supramolecular Self-Assemblies for Cancer Theranostics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  18. Article
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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

13 authors.

Jie LiDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA).
Yi KuangDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA).
Junfeng ShiDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA).
Jie ZhouDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA).
Jamie E MedinaDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115 (USA).
Rong ZhouDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA).
Dan YuanDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA).
Cuihong YangTianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science and Peking Union Medical College, Tianjin 300192 (P.R. China).
Huaimin WangState Key Laboratory of Medicinal Chemical Biology and College of Life Sciences, Nankai University, Tianjin 300071 (China).
Zhimou YangState Key Laboratory of Medicinal Chemical Biology and College of Life Sciences, Nankai University, Tianjin 300071 (China).
Jianfeng LiuTianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science and Peking Union Medical College, Tianjin 300192 (P.R. China).
Daniela M DinulescuDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115 (USA). ddinulescu@rics.bwh.harvard.edu.
Bing XuDepartment of Chemistry, Brandeis University, 415 South St, Waltham, MA 02454 (USA). bxu@brandeis.edu.

Funding

Subcellular Enzyme-instructed self-assembly for molecular anticancer nanomedicinesR01CA142746 · NCI · BRANDEIS UNIVERSITY · PI Bing Xu · 2010 to 2026
$6.4M
Defining microRNA Signatures for Early Detection in BRCA-Mutated Ovarian CancerR03CA189462 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI DINULESCU, DANIELA M · 2014 to 2015
$170k
NCI NIH HHS R01 CA142746NCI NIH HHS R03 CA189462PHS HHS R01A142746
6 · The paper itself

Abstract

Anticancer drug resistance demands innovative approaches that boost the activity of drugs against drug-resistant cancers without increasing the systemic toxicity. Here we show the use of enzyme-instructed self-assembly (EISA) to generate intracellular supramolecular assemblies that drastically boost the activity of cisplatin against drug-resistant ovarian cancer cells. We design and synthesize small peptide precursors as the substrates of carboxylesterase (CES). CES cleaves the ester bond pre-installed on the precursors to form the peptides that self-assemble in water to form nanofibers. At the optimal concentrations, the precursors themselves are innocuous to cells, but they double or triple the activity of cisplatin against the drug-resistant ovarian cancer cells. This work illustrates a simple, yet fundamental, new way to introduce non-cytotoxic components into combination therapies with cisplatin without increasing the systemic burden or side effects.

Indexed as

Antineoplastic AgentsCarboxylesteraseCell Line, TumorCell SurvivalCisplatinDose-Response Relationship, DrugDrug Resistance, NeoplasmFemaleHumansMolecular StructureOvarian NeoplasmsPeptidesStructure-Activity RelationshipAntineoplastic AgentsCarboxylesteraseCisplatinPeptidescisplatincombination therapydrug-resistanceenzymesself-assembly

Identifiers

PMID26365295
PMCPMC4681442

What OpenQuestion holds

Textmetadata
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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.