Evidence map›Paper›PMID 37673917›Full record

ArticleNature communications2023

Optogenetic engineering of STING signaling allows remote immunomodulation to enhance cancer immunotherapy.

Yaling Dou, Rui Chen, Siyao Liu, Yi-Tsang Lee, Ji Jing, Xiaoxuan Liu, Yuepeng Ke, Rui Wang, Yubin Zhou, Yun Huang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  5. Chemical reviews · 2026
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  16. From Bench to Bedside: Emerging Paradigms in CAR-T Cell Therapy for Solid Malignancies.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  17. Optogenetic engineering for precision cancer immunotherapy.Trends in pharmacological sciences · 2025
    Review
  18. Review
  19. Article
  20. Review
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

10 authors at 1 institution in 1 country.

Yaling Dou *Institute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Rui Chen *Institute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Siyao LiuInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Yi-Tsang LeeInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.ORCID http://orcid.org/0000-0003-4515-0355
Ji JingInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Xiaoxuan LiuInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Yuepeng KeInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Rui WangInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Yubin ZhouInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA. yubinzhou@tamu.edu.ORCID http://orcid.org/0000-0001-7962-0517
Yun HuangInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA. yun.huang@tamu.edu.ORCID http://orcid.org/0000-0001-5950-9168
Texas A&M University · US

Funding

Epigenetic regulation in cardiac developmentR35HL166557 · NHLBI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI Yun Huang · 2023 to 2026
$3.8M
Mutational cooperativity in TET2-associated hematological malignancies.R01CA240258 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HUANG, YUN · 2021 to 2025
$1.7M
Engineering Smart Antibody-like Protein Scaffolds with precision switchesR01GM144986 · NIGMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ZHOU, YUBIN · 2022 to 2025
$1.3M
Synthetic biology toolkit for precise tuning of T cell activityR21AI174606 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ZHOU, YUBIN · 2023 to 2024
$417k
NCI NIH HHS R01 CA240258NHLBI NIH HHS R35 HL166557NIAID NIH HHS R21 AI174606NIGMS NIH HHS R01 GM144986
6 · The paper itself

Abstract

The cGAS-STING signaling pathway has emerged as a promising target for immunotherapy development. Here, we introduce a light-sensitive optogenetic device for control of the cGAS/STING signaling to conditionally modulate innate immunity, called 'light-inducible SMOC-like repeats' (LiSmore). We demonstrate that photo-activated LiSmore boosts dendritic cell (DC) maturation and antigen presentation with high spatiotemporal precision. This non-invasive approach photo-sensitizes cytotoxic T lymphocytes to engage tumor antigens, leading to a sustained antitumor immune response. When combined with an immune checkpoint blocker (ICB), LiSmore improves antitumor efficacy in an immunosuppressive lung cancer model that is otherwise unresponsive to conventional ICB treatment. Additionally, LiSmore exhibits an abscopal effect by effectively suppressing tumor growth in a distal site in a bilateral mouse model of melanoma. Collectively, our findings establish the potential of targeted optogenetic activation of the STING signaling pathway for remote immunomodulation in mice.

Indexed as

NeoplasmsOptogeneticsAnimalsAntigen PresentationChromogranin AImmunomodulationImmunotherapyMiceNucleotidyltransferasesChromogranin ANucleotidyltransferases

Identifiers

PMID37673917
PMCPMC10482946
OpenAlexW4386482910

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.