Evidence map›Paper›PMID 38261737›Full record

ArticleAging2024

CDK16 as a potential prognostic biomarker correlated with an immunosuppressive tumor microenvironment and benefits in enhancing the effectiveness of immunotherapy in human cancers.

Juntao Qi, Gujie Wu, Min He, You Xu, Zheng Yang, Liang Ding, Yan Wang, Zhi Zhang

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 1 country.

Juntao QiDepartment of Urology, Shenzhen Hospital of Shanghai University of Traditional Chinese Medicine, Shenzhen 518000, China.
Gujie WuResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226000, China.
Min HeResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226000, China.
You XuResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226000, China.
Zheng YangResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226000, China.
Liang DingResearch Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226000, China.
Yan WangDepartment of Urology, Shenzhen Hospital of Shanghai University of Traditional Chinese Medicine, Shenzhen 518000, China.
Zhi ZhangDepartment of Health Management, The First Hospital of Hunan University of Chinese Medicine, Changsha, Hunan 410000, China.
Nantong University · CNAffiliated Hospital of Nantong University · CNShanghai University of Traditional Chinese Medicine · CNHunan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCyclin-Dependent Kinase 16 (CDK16) plays significant biological roles in various diseases. Nonetheless, its function in different cancer types and its relationship with the Tumor Immune Microenvironment (TIME) are still not well-understood.

methodsWe analyzed the expression profile, genetic alterations, clinical features, and prognostic value of CDK16 in pan-cancer using data from The Cancer Genome Atlas, Genotype-Tissue Expression databases, and

resultsCDK16 is notably overexpressed in pan-cancer and is a risk factor for poor prognosis in various cancers. Our findings reveal that CDK16 regulates not only cell cycle-related functions to promote cell proliferation but also the autoimmunity-related functions of the innate and adaptive immune systems, along with other immune-related signaling pathways. Moreover, CDK16 overexpression contributes to an immunosuppressive tumor microenvironment, extensively suppressing immune-related features such as the expression of immune-related genes and pathways, as well as the count of immune-infiltrating cells. Our analysis indicated that individuals with low CDK16 expression showed higher response rates to immune checkpoint inhibitors and longer overall survival compared to those with high CDK16 expression.

conclusionsThis study establishes CDK16 as a potential biomarker for predicting poor prognosis in a wide range of cancers. Its role in shaping the immunosuppressive tumor microenvironment and influencing the efficacy of immunotherapy highlights the urgent need for developing targeted therapies against CDK16, offering new avenues for cancer treatment and management.

Indexed as

NeoplasmsTumor MicroenvironmentCyclin-Dependent KinasesGenes, cdcHumansImmunotherapyPrognosisCyclin-Dependent KinasesCDK16human cancersimmunosuppressive tumor microenvironmentimmunotherapyprognosis

Identifiers

PMID38261737
PMCPMC10866429
OpenAlexW4391104732

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.