Evidence map›Paper›PMID 39141816›Full record

ArticleACS nano2024

Targeting Tumor-Associated Macrophages with the Immune-Activating Nanomedicine for Achieving Strong Antitumor Activity with Rapid Clearance from the Body.

Yosuke Ota, Ryosaku Inagaki, Yosuke Takanashi, Hiro Uemachi, Kimiya Matsuda, Makoto Matsuoka, Risa Taoda, Seina Ohe, Yukari Ishitsubo, Megumi Nakamura and 3 more

Abstract read
In one paragraph

Article in ACS nano, 2024. 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
–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

11 citing papers in PubMed.

  1. Review
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  3. Article
  4. Article
  5. Review
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  7. Tumor-associated macrophages and platelets in tumor microenvironment and its potential therapeutic role in ovarian cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  8. Article
  9. 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

13 authors.

Yosuke OtaCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Ryosaku InagakiCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Yosuke TakanashiModality Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Hiro UemachiModality Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Kimiya MatsudaCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Makoto MatsuokaModality Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Risa TaodaCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Seina OheCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Yukari IshitsuboCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Megumi NakamuraCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Masashi GotoCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Hitoshi BanOncology, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.
Yasuhiro NagaiCancer Research Unit, Sumitomo Pharma Co Ltd, Osaka 5540022, Japan.ORCID 0009-0004-8373-2908

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are a class of pattern recognition receptors (PRRs) crucial for the detection of infections and activation of downstream signaling pathways that lead to the production of pro-inflammatory cytokines and interferons. The TLR pathway is an attractive actively studied target pathway. Because of their strong immunostimulatory activity, TLRs are thought to be a "double-edged sword" for systemic treatment, even in the cancer field. To solve this, we have developed dextran-based TAM targeting activating conjugate (D-TAC) technology, which successfully uses tumor-associated macrophages (TAMs) to deliver the TLR7 agonist DSP-0509. We used low molecular weight dextran to target CD206 high M2-type macrophages, activate them, and induce a change in phenotype to antitumor M1-type macrophages with rapid clearance from the body and astonishing antitumor activity. We also demonstrated that the antitumor effect of our best drug candidate 5DEX-0509R is dependent on the abundance of TAMs, which is consistent with their mechanism of action. We believe that 5DEX-0509R generated by D-TAC technology can be a clinically applicable immunotherapy targeting the TLR signaling pathway.

Indexed as

Antineoplastic AgentsNanomedicineToll-Like Receptor 7Tumor-Associated MacrophagesAnimalsCell Line, TumorDextransFemaleHumansMacrophagesMiceMice, Inbred C57BLAntineoplastic AgentsDextransToll-Like Receptor 7cancer immunologynanomedicine, TLR7. tumor microenvironmenttumor associated macrophages

Identifiers

PMID39141816
PMCPMC11363121

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.