Evidence map›Paper›PMID 31956823›Full record

ArticleACS omega2020

Oxaliplatin-Based Platinum(IV) Prodrug Bearing Toll-like Receptor 7 Agonist for Enhanced Immunochemotherapy.

Li Tang, Demin Cai, Mian Qin, Shuo Lu, Ming-Hao Hu, Shuangchen Ruan, Guangyi Jin, Zhigang Wang

Abstract read
In one paragraph

Article in ACS omega, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Improved Systemic Immunochemotherapy Employing an Oxaliplatin-TLR7/8 Agonist Prodrug Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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.

Li TangSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Demin CaiSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Mian QinSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Shuo LuSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Ming-Hao HuSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Shuangchen RuanSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Guangyi JinSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.
Zhigang WangSchool of Pharmaceutical Sciences, Health Science Center, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, International Cancer Center, Health Science Center, and The National-Regional Engineering Lab for Synthetic Biology of Medicine, Health Science Center, Shenzhen University, Shenzhen 518060, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A combination of platinum drugs with immunotherapy has shown promising anticancer effects, especially in the drug resistance cancer model. Herein, a new type of immunochemotherapeutic was designed by tethering the toll-like receptor 7 (TLR7) agonist on the axial position of oxaliplatin-based platinum(IV) prodrug. The prodrug simultaneously induced immunogenic cell death of 4T1 cancer cells to initiate an immune response and activate dendritic cells (DCs) to secrete proinflammatory cytokines including interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and IL-12, to further enhance the adaptive immunity. The prodrug exhibited better in vivo anticancer effects than oxaliplatin in the 4T1 allograft mouse model, a later stage breast cancer model, which showed poor response to traditional chemotherapy. Mechanism studies revealed that enhanced activation of cytotoxic T cells within tumor contribute to the high in vivo anticancer efficiency of the prodrug. Moreover, the prodrug displayed much lower cytotoxicity to DCs compared with oxaliplatin, indicating its safety to normal cells. These results highlight the potential of the conjugation of TLR7 agonist with oxaliplatin-based Pt(IV) prodrug as an effective anticancer agent to overcome the toxic side effects and drug resistance of traditional platinum chemotherapy.

Identifiers

PMID31956823
PMCPMC6964279

What OpenQuestion holds

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Registered trials

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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.