Evidence map›Paper›PMID 36468774›Full record

ReviewCancer science2023

The cancer epigenome: Non-cell autonomous player in tumor immunity.

Shinichiro Kato, Yuka Maeda, Daisuke Sugiyama, Keisuke Watanabe, Hiroyoshi Nishikawa, Kunihiko Hinohara

Open access · goldAbstract readReview
In one paragraph

Review in Cancer science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

6 citing papers in PubMed, 3 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

6 authors at 2 institutions in 1 country.

Shinichiro KatoDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yuka MaedaDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Research Institute, Tokyo, Japan.
Daisuke SugiyamaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Keisuke WatanabeDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6539-2549
Hiroyoshi NishikawaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0001-6563-9807
Kunihiko HinoharaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0002-7099-9441
Nagoya University · JPNagoya University Hospital · JP

Funding

Japan Agency for Medical Research and Development 19ae0101074s0401Japan Agency for Medical Research and Development 22ck0106724h0001Japan Agency for Medical Research and Development 22ck0106772h0001Japan Agency for Medical Research and Development JP20cm0106166h0002Japan Agency for Medical Research and Development JP20cm0106703h0001Japan Agency for Medical Research and Development JP22ama221110h0001Japan Agency for Medical Research and Development JP22ama221301h0001Japan Agency for Medical Research and Development JP22cm0106186h0002Japan Society for the Promotion of Science JP20H03512Japan Society for the Promotion of Science JP20KJapan Society for the Promotion of Science JP20K16301Japan Society for the Promotion of Science JP22K07148Japan Society for the Promotion of Science JP22K1
6 · The paper itself

Abstract

Dysregulation of the tumor-intrinsic epigenetic circuit is a key driver event for the development of cancer. Accumulating evidence suggests that epigenetic and/or genetic drivers stimulate intrinsic oncogenic pathways as well as extrinsic factors that modulate the immune system. These modulations indeed shape the tumor microenvironment (TME), allowing pro-oncogenic factors to become oncogenic, thereby contributing to cancer development and progression. Here we review the epigenetic dysregulation arising in cancer cells that disseminates throughout the TME and beyond. Recent CRISPR screening has elucidated key epigenetic drivers that play important roles in the proliferation of cancer cells (intrinsic) and inhibition of antitumor immunity (extrinsic), which lead to the development and progression of cancer. These epigenetic players can serve as promising targets for cancer therapy as a dual (two-in-one)-targeted approach. Considering the interplay between cancer and the immune system as a key determinant of immunotherapy, we discuss a novel lineage-tracing technology that enables longitudinal monitoring of cancer and immune phenotypic heterogeneity and fate paths during cancer development, progression, and therapeutic interventions.

Indexed as

EpigenomeNeoplasmsHumansImmunotherapyTumor Microenvironmentantitumor immunitydual-targeted cancer therapyepigenetic reprogramminghistone modificationimmune system

Identifiers

PMID36468774
PMCPMC9986067
OpenAlexW4310705464

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.