Evidence map›Paper›PMID 37928953›Full record

ArticleInternational journal of general medicine2023

Role of Kinetochore Scaffold 1 (KNL1) in Tumorigenesis and Tumor Immune Microenvironment in Pan-Cancer: Bioinformatics Analyses and Validation of Expression.

Yixin Ding, Kongjia Wang, Shufen Zhao, Yu Li, Wensheng Qiu, Chunyang Zhu, Yan Wang, Chen Dong, Jiani Liu, Yangyang Lu and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of general medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 4 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

11 authors at 1 institution in 1 country.

Yixin Ding *Department of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Kongjia Wang *Department of Urology, Qingdao Municipal Hospital, Qingdao University, Qingdao, People's Republic of China.ORCID 0009-0002-0995-409X
Shufen ZhaoDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Yu LiDepartment of Gastrointestinal Surgery, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Wensheng QiuDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Chunyang ZhuDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Yan WangDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Chen DongDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Jiani LiuDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Yangyang LuDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Weiwei QiDepartment of Oncology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Kinetochore scaffold 1 (KNL1), a crucial protein during cell mitosis participating in cell division, was widely expressed in multiple kinds of cancers. However, the expression profile, the effect on cell biological function, tumor immune microenvironment, and predictive value of clinical prognosis in pan-cancer of KNL1 still require a comprehensive inquiry. Methods: The mRNA and protein expression profile of KNL1 was validated in pan-cancer using different databases. Six algorithms were used to explore the correlation between KNL1 and immune infiltration and the relationship between KNL1 and tumor mutation burden (TMB), microsatellite instability (MSI), and TIDE score were calculated. The diagnostic and clinical prognostic predictive ability of KNL1 was assessed. Differentially expressed genes (DEGs) of KNL1 were screened out and function enrichment analyses were performed in pancreatic adenocarcinoma (PAAD), stomach adenocarcinoma (STAD), and bladder urothelial carcinoma (BLCA). Finally, 8 cases of pancreatic adenocarcinoma tissues and paired adjacent tissues were collected for immunohistochemical (IHC) staining and the histological score (H-score) was calculated. Real-time PCR was performed in gastric cancer and bladder cancer cell lines. Results: KNL1 was abnormally upregulated in more than half of cancers across different databases. IHC and real-time PCR verified the up-regulated expression in cancer tissues in PAAD, gastric cancer, and BLCA. The satisfactory diagnostic value of KNL1 was indicated in 30 cancers and high KNL1 expression was associated with poorer overall survival (OS) in 12 cancers. The prognostic role of KNL1 as a predictive biomarker of PAAD was clarified. KNL1 played an active part in the cell cycle and cell proliferation. Moreover, KNL1 was likely to mold the Th2-dominant suppressive tumor immune microenvironment and was associated with TMB, MSI, and immune checkpoint-related genes in pan-cancer. Conclusion: Our study elucidated the anomalous expression of KNL1 and revealed that KNL1 was a promising prognostic biomarker in pan-cancer.

Indexed as

bioinformaticsclinical prognostic modelimmune infiltrationKNL1pan-cancerprognosis

Identifiers

PMID37928953
PMCPMC10625436
OpenAlexW4388024718

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