Evidence map›Paper›PMID 33013881›Full record

ArticleFrontiers in immunology2020

Tumor-Derived cGAMP Regulates Activation of the Vasculature.

Marco Campisi, Shriram K Sundararaman, Sarah E Shelton, Erik H Knelson, Navin R Mahadevan, Ryohei Yoshida, Tetsuo Tani, Elena Ivanova, Israel Cañadas, Tatsuya Osaki and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

41 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
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  8. Restoration of cGAS in cancer cells promotes antitumor immunity via transfer of cancer cell-generated cGAMP.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  12. STING Agonists and How to Reach Their Full Potential in Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  18. Advancements in preclinical human-relevant modeling of pulmonary vasculature on-chip.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2024
    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

20 authors at 6 institutions in 4 countries.

Marco CampisiDepartment of Mechanical and Aerospace Engineering, Politecnico di Torino, Turin, Italy.
Shriram K SundararamanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Sarah E SheltonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Erik H KnelsonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Navin R MahadevanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Ryohei YoshidaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Tetsuo TaniDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Elena IvanovaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Israel CañadasDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Tatsuya OsakiDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, United States.
Sharon Wei Ling LeeSingapore-MIT Alliance for Research & Technology, BioSystems and Micromechanics, Singapore, Singapore.
Tran ThaiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Saemi HanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Brandon P PielDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Sean GilhooleyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Cloud P PaweletzDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Valeria ChionoDepartment of Mechanical and Aerospace Engineering, Politecnico di Torino, Turin, Italy.
Roger D KammDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, United States.
Shunsuke KitajimaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
David A BarbieDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States.
Dana-Farber Cancer Institute · USMassachusetts Institute of Technology · USPolytechnic University of Turin · ITFox Chase Cancer Center · USJapanese Foundation For Cancer Research · JPSingapore-MIT Alliance for Research and Technology · SG

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI Deborah J Goff · 1985 to 2026
$330.6M
Development of Physiologic Tissue Models to Assess Tumor Explant Response to Immune Checkpoint BlockadeU01CA214381 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BARBIE, DAVID A, KAMM, ROGER D · 2017 to 2021
$3.5M
Imaging Cancer Angiogenesis with Acoustic Angiography UltrasoundK00CA212227 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SHELTON, SARAH ELIZABETH · 2018 to 2021
$392k
NCI NIH HHS K00 CA212227NCI NIH HHS P30 CA006516NCI NIH HHS U01 CA214381
6 · The paper itself

Abstract

Intratumoral recruitment of immune cells following innate immune activation is critical for anti-tumor immunity and involves cytosolic dsDNA sensing by the cGAS/STING pathway. We have previously shown that KRAS-LKB1 (KL) mutant lung cancer, which is resistant to PD-1 blockade, exhibits silencing of STING, impaired tumor cell production of immune chemoattractants, and T cell exclusion. Since the vasculature is also a critical gatekeeper of immune cell infiltration into tumors, we developed a novel microfluidic model to study KL tumor-vascular interactions. Notably, dsDNA priming of LKB1-reconstituted tumor cells activates the microvasculature, even when tumor cell STING is deleted. cGAS-driven extracellular export of 2'3' cGAMP by cancer cells activates STING signaling in endothelial cells and cooperates with type 1 interferon to increase vascular permeability and expression of E selectin, VCAM-1, and ICAM-1 and T cell adhesion to the endothelium. Thus, tumor cell cGAS-STING signaling not only produces T cell chemoattractants, but also primes tumor vasculature for immune cell escape.

Indexed as

Lung NeoplasmsNeovascularization, PathologicSignal TransductionCell Line, TumorCoculture TechniquesEndothelial CellsHumansNeoplasm ProteinsNucleotides, Cycliccyclic guanosine monophosphate-adenosine monophosphateNeoplasm ProteinsNucleotides, Cyclic2′3′-cGAMPendothelial cellsKRASLKB1microfluidic cultureSTINGT cell

Identifiers

PMID33013881
PMCPMC7507350
OpenAlexW3083704567

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.