Evidence map›Paper›PMID 34471678›Full record

ArticleACS central science2021

Modulation of Siglec-7 Signaling Via In Situ-Created High-Affinity

Senlian Hong, Chenhua Yu, Emily Rodrigues, Yujie Shi, Hongmin Chen, Peng Wang, Digantkumar G Chapla, Tao Gao, Ruoxuan Zhuang, Kelley W Moremen and 3 more

Open access · diamondAbstract read
In one paragraph

Article in ACS central science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 44 citations in OpenAlex.

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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 at 4 institutions in 3 countries.

Senlian HongState Key Laboratory of Natural and Biomimetic Drugs, Chemical Biology Center, Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Chenhua YuDepartment of Molecular Medicine, Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla 92037, California, United States.
Emily RodriguesDepartment of Chemistry, Department of Medical Microbiology and Immunology, University of Alberta, 11227 Saskatchewan Drive NW, Edmonton AB T6G 2G2, Alberta, Canada.
Yujie ShiDepartment of Molecular Medicine, Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla 92037, California, United States.
Hongmin ChenState Key Laboratory of Natural and Biomimetic Drugs, Chemical Biology Center, Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Peng WangDepartment of Molecular Medicine, Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla 92037, California, United States.
Digantkumar G ChaplaComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia 30602, United States.
Tao GaoState Key Laboratory of Natural and Biomimetic Drugs, Chemical Biology Center, Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Ruoxuan ZhuangState Key Laboratory of Natural and Biomimetic Drugs, Chemical Biology Center, Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Kelley W MoremenComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia 30602, United States.
James C PaulsonDepartment of Molecular Medicine, Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla 92037, California, United States.ORCID https://orcid.org/0000-0003-4589-5322
Matthew S MacauleyDepartment of Chemistry, Department of Medical Microbiology and Immunology, University of Alberta, 11227 Saskatchewan Drive NW, Edmonton AB T6G 2G2, Alberta, Canada.ORCID https://orcid.org/0000-0003-4579-1048
Peng WuDepartment of Molecular Medicine, Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla 92037, California, United States.ORCID https://orcid.org/0000-0002-5204-0229
Scripps Research Institute · USPeking University · CNUniversity of Alberta · CAUniversity of Georgia · US

Funding

Treating lung inflammation by targeting SiglecsP01HL107151 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SCHNAAR, RONALD L · 2011 to 2017
$15.4M
TR&D3. Approaches to Proteoglycan Function at Biochemical and Cellular LevelsP41GM103390 · NIGMS · UNIVERSITY OF GEORGIA · PI MOREMEN, KELLEY W. · 2012 to 2019
$14.5M
Using siglecs and their ligands to treat allergic diseases SALTADU19AI136443 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BOCHNER, BRUCE S · 2018 to 2022
$7.6M
Recombinant Production of Glycosylation Enzymes for Biochem/Structural StudiesP01GM107012 · NIGMS · UNIVERSITY OF GEORGIA · PI PRESTEGARD, JAMES H. · 2013 to 2017
$7.5M
REGULATION OF SIALOSIDE EXPRESSION IN LEUKOCYTESR01AI050143 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2003 to 2018
$7.0M
Exploring Siglec-glycan ligand interactions using chemoenzymatic approachesR01AI154138 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI WU, PENG · 2021 to 2025
$4.1M
Origin of N-Glycan Site-Specific HeterogeneityR01GM130915 · NIGMS · UNIVERSITY OF GEORGIA · PI KANNAN, NATARAJAN, MOREMEN, KELLEY W. · 2019 to 2022
$3.4M
Glycan dependent epitopes of HIV broadly neutralizing antibodiesR56AI113867 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C, SCHIEF, WILLIAM R. · 2020 to 2020
$887k
NHLBI NIH HHS P01 HL107151NIAID NIH HHS R01 AI050143NIAID NIH HHS R01 AI154138NIAID NIH HHS R56 AI113867NIAID NIH HHS U19 AI136443NIGMS NIH HHS P01 GM107012NIGMS NIH HHS P41 GM103390NIGMS NIH HHS R01 GM130915
6 · The paper itself

Abstract

Sialic acid-binding immunoglobulin-like lectins, also known as Siglecs, have recently been designated as glyco-immune checkpoints. Through their interactions with sialylated glycan ligands overexpressed on tumor cells, inhibitory Siglecs on innate and adaptive immune cells modulate signaling cascades to restrain anti-tumor immune responses. However, the elucidation of the mechanisms underlying these processes is just beginning. We find that when human natural killer (NK) cells attack tumor cells, glycan remodeling occurs on the target cells at the immunological synapse. This remodeling occurs through both the transfer of sialylated glycans from NK cells to target tumor cells and the accumulation of

Identifiers

PMID34471678
PMCPMC8393205
OpenAlexW3194694436

What OpenQuestion holds

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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.