Evidence map›Paper›PMID 38162677›Full record

ReviewFrontiers in genetics2023

Unveiling immune checkpoint regulation: exploring the power of

Yuxiang Wang, Athar Khalil, Amina Kamar, Mengyan Du, Trang Dinh, Christopher McFarland, Zhenghe Wang

Abstract readReview
In one paragraph

Review in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

7 authors.

Yuxiang Wang *Department of Genetics and Genome Sciences and Case Comprehesive Cancer Center, Case Western Reserve University, Cleveland, OH, United States.
Athar Khalil *Department of Genetics and Genome Sciences and Case Comprehesive Cancer Center, Case Western Reserve University, Cleveland, OH, United States.
Amina KamarCentre for Digital Transformation, Imperial College, London, United Kingdom.
Mengyan DuDepartment of Genetics and Genome Sciences and Case Comprehesive Cancer Center, Case Western Reserve University, Cleveland, OH, United States.
Trang DinhDepartment of Genetics and Genome Sciences and Case Comprehesive Cancer Center, Case Western Reserve University, Cleveland, OH, United States.
Christopher McFarlandDepartment of Genetics and Genome Sciences and Case Comprehesive Cancer Center, Case Western Reserve University, Cleveland, OH, United States.
Zhenghe WangDepartment of Genetics and Genome Sciences and Case Comprehesive Cancer Center, Case Western Reserve University, Cleveland, OH, United States.

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Amar Desai · 1987 to 2026
$142.3M
Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
Mechanisms of metabolic reprogramming by PIK3CA oncogenic mutationsR01CA196643 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Zhenghe Wang · 2016 to 2026
$3.1M
Role of Erbb3 kinase activity in colorectal tumorigenesis.R01CA256791 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2021 to 2025
$2.5M
Tumor-barcoding coupled with high-throughput sequencing for quantitative radiogenomics of the abscopal response in NSCLCR01CA271540 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Phuoc T. Tran · 2023 to 2026
$2.3M
Role of PTPRT in colon cancer progression and metastasisR01CA260629 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2022 to 2025
$2.2M
Mechanisms of PIK3CA helical domain mutations driving colorectal tumorigenesisR01CA264320 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2021 to 2025
$2.0M
Quantifying the sources and dynamics of tumor growth variability using Tuba-seqR00CA226506 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MCFARLAND, CHRISTOPHER DENNIS · 2021 to 2023
$747k
NCI NIH HHS P30 CA043703NCI NIH HHS P50 CA150964NCI NIH HHS R00 CA226506NCI NIH HHS R01 CA196643NCI NIH HHS R01 CA256791NCI NIH HHS R01 CA260629NCI NIH HHS R01 CA264320NCI NIH HHS R01 CA271540
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) have revolutionized cancer immunotherapy by reinvigorating antitumor immune responses, but their efficacy remains limited in most patients. To address this challenge and optimize Immune check inhibitor treatment, understanding the underlying molecular intricacies involved is crucial. The emergence of CRISPR-Cas9 technology has empowered researchers to precisely investigate gene function and has introduced transformative shifts in identifying key genes for various physiological and pathological processes. CRISPR screenings, particularly

Indexed as

CRISPR (clustered regularly interspaced short palindromic repeat)/Cas9 (CRISPR associated protein 9)-mediated genome editingCTLA-4immune check inhibitor (ICI)invitro CRISPR screenin vivo CRISPR screenPD-1tumor immunotherapy

Identifiers

PMID38162677
PMCPMC10755878

What Socratic 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 Socratic graph.