Evidence map›Paper›PMID 38648067›Full record

ArticleMolecular cancer therapeutics2024

Antitumor Activity of a Novel LAIR1 Antagonist in Combination with Anti-PD1 to Treat Collagen-Rich Solid Tumors.

Bertha L Rodriguez, Jiawei Huang, Laura Gibson, Jared J Fradette, Hung-I H Chen, Kikuye Koyano, Czrina Cortez, Betty Li, Carmence Ho, Amir M Ashique and 11 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. The Multifaced Role of Collagen in Cancer Development and Progression.International journal of molecular sciences · 2024
    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

21 authors at 2 institutions in 1 country.

Bertha L RodriguezDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8406-7509
Jiawei HuangNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0008-9721-828X
Laura GibsonDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0003-1668-6898
Jared J FradetteDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-6712-2860
Hung-I H ChenNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0000-0003-2760-2258
Kikuye KoyanoNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0000-0002-5250-9293
Czrina CortezNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0000-5428-991X
Betty LiNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0006-7293-9465
Carmence HoNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0005-0042-5230
Amir M AshiqueNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0008-5107-8090
Vicky Y LinNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0000-9324-4933
Suzanne CrawleyNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0007-6411-1294
Julie M RodaNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0000-0001-5631-9908
Peirong ChenNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0008-3293-3426
Bin FanNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0002-8928-6844
Jeong KimNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0006-1422-9203
James SissonsNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0000-9312-128X
Jonathan SitrinNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0009-0001-2496-5793
Daniel D KaplanNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0000-0001-8297-560X
Don L GibbonsDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0003-2362-3094
Lee B RiveraNGM Biopharmaceuticals Inc., South San Francisco, California.ORCID 0000-0003-2658-1862
NGM Biopharmaceuticals (United States) · USThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V., MINNA, JOHN D. · 1996 to 2024
$57.4M
Cancer Prevention and Research Institute of Texas (CPRIT) RP200235National Cancer Institute (NCI) P50CA070907NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907
6 · The paper itself

Abstract

We recently reported that resistance to PD-1 blockade in a refractory lung cancer-derived model involved increased collagen deposition and the collagen-binding inhibitory receptor leukocyte-associated immunoglobulin-like receptor 1 (LAIR1). Thus, we hypothesized that LAIR1 and collagen cooperated to suppress therapeutic response. In this study, we report that LAIR1 is associated with tumor stroma and is highly expressed by intratumoral myeloid cells in both human tumors and mouse models of cancer. Stroma-associated myeloid cells exhibit a suppressive phenotype and correlate with LAIR1 expression in human cancer. NGM438, a novel humanized LAIR1 antagonist mAb, elicits myeloid inflammation and allogeneic T-cell responses by binding to LAIR1 and blocking collagen engagement. Furthermore, a mouse-reactive NGM438 surrogate antibody sensitized refractory KP mouse lung tumors to anti-PD-1 therapy and resulted in increased intratumoral CD8+ T-cell content and inflammatory gene expression. These data place LAIR1 at the intersection of stroma and suppressive myeloid cells and support the notion that blockade of the LAIR1/collagen axis can potentially address resistance to checkpoint inhibitor therapy in the clinic.

Indexed as

Antineoplastic AgentsCollagenImmune Checkpoint InhibitorsReceptors, ImmunologicAnimalsCell Line, TumorDisease Models, AnimalFemaleHumansLung NeoplasmsMiceNeoplasmsProgrammed Cell Death 1 ReceptorAntineoplastic AgentsCollagenImmune Checkpoint Inhibitorsleukocyte-associated immunoglobulin-like receptor 1Programmed Cell Death 1 ReceptorReceptors, Immunologic

Identifiers

PMID38648067
PMCPMC11293989
OpenAlexW4395012336

What OpenQuestion holds

Textmetadata
LicenceTDM
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.