Evidence map›Paper›PMID 41341044›Full record

ArticleACS central science2025

Reshaping Tumor-Lymph Node Immune Axis via Targeted Lymphatic Delivery of Dual-Functional Immune Modulator for Enhanced Cancer Immunotherapy.

Su Yeon Lim, Pin Liu, Ju Hwa Shin, Bum Soo Lee, Sun Ju Kim, Dahwun Kim, Siyan Lyu, Byung Deok Kim, Chaeeun Park, Junku Jung and 8 more

Abstract read
In one paragraph

Article in ACS central science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Su Yeon LimSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Pin LiuSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Ju Hwa ShinSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Bum Soo LeeSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Sun Ju KimSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Dahwun KimSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Siyan LyuSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Byung Deok KimSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Chaeeun ParkSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Junku JungSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Jihyun LeeSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Jinbeom SeoSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Taegwan YunSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Hyo Jin ParkSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Min Sang LeeSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Ki Hyun KimSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID https://orcid.org/0000-0002-5285-9138
Wonsik LeeSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Ji Hoon JeongSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID https://orcid.org/0000-0002-4836-3551

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of cancer immunotherapy is often limited by the immunosuppressive tumor microenvironment (TME) and insufficient immune activation in tumor-draining lymph nodes (TDLN). Since the TME and TDLN form a dynamic axis crucial for tumor metastasis and resistance to immune checkpoint blockade, strategies that effectively modulate both sites are critical. Here, we present a dissolving microneedle (MN) system that generates nanomicelles (NMCs) for localized delivery of a newly identified dual-functional macrocyclic trichothecene, Roridin E (R.E). R.E induces cancer cell-autonomous secretion of IFN-β and immunogenic cancer cell death (ICD). Direct delivery of R.E to the TDLN via the MN platform reshapes the local immune landscape to suppress cancer while minimizing off-target toxicity. In a B16F10 melanoma model, MN-guided R.E. delivery significantly improved tumor control, reduced lung metastases, and extended overall survival. This approach provides a minimally invasive and effective strategy for integrating natural-product-based therapies with advanced drug delivery systems to target the TME-TDLN axis, thereby improving outcomes in metastatic cancer.

Identifiers

PMID41341044
PMCPMC12670315

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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.