Evidence mapPaperPMID 39008137Full record

ReviewMedical oncology (Northwood, London, England)2024

The multifaceted role of PCSK9 in cancer pathogenesis, tumor immunity, and immunotherapy.

Chou-Yi Hsu, Mustafa Nasrat Abdulrahim, Mohammed Ahmed Mustafa, Thabit Moath Omar, Franklin Balto, Indira Pineda, Teeba Thamer Khudair, Mohammed Ubaid, Mohammed Shnain Ali

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
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  3. [Research progress on poor response, resistance mechanisms, and influencing factors of immunotherapy for hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
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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

9 authors.

Chou-Yi HsuDepartment of Pharmacy, Chia Nan University of Pharmacy and Science, Tainan City, 71710, Taiwan. chouyihsu6@gmail.com.
Mustafa Nasrat AbdulrahimCollege of Education, University of Anbar, AL Qaim, Iraq.
Mohammed Ahmed MustafaDepartment of Medical Laboratory Technology, Imam Jaafar AL-Sadiq University, Baghdad, Iraq.
Thabit Moath OmarDepartment of Medical Laboratory Technics, Al-Noor University College, Nineveh, Iraq.
Franklin BaltoDepartment of Biotechnology and Genetics, Jain (Deemed-to-be) University, Bengaluru, Karnataka, 560069, India.
Indira PinedaSchool of Basic & Applied Sciences, Shobhit University, Gangoh, Uttar Pradesh, 247341, India.
Teeba Thamer KhudairCollege of Nursing, National University of Science and Technology, Dhi Qar, Iraq.
Mohammed UbaidMedical Technical College, Al-Farahidi University, Baghdad, Iraq.
Mohammed Shnain AliDepartment of Dentistry, Al-Zahrawi University College, Karbala, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9), a well-known regulator of cholesterol metabolism and cardiovascular diseases, has recently garnered attention for its emerging involvement in cancer biology. The multifunctional nature of PCSK9 extends beyond lipid regulation and encompasses a wide range of cellular processes that can influence cancer progression. Studies have revealed that PCSK9 can modulate signaling pathways, such as PI3K/Akt, MAPK, and Wnt/β-catenin, thereby influencing cellular proliferation, survival, and angiogenesis. Additionally, the interplay between PCSK9 and cholesterol homeostasis may impact membrane dynamics and cellular migration, further influencing tumor aggressiveness. The central role of the immune system in monitoring and controlling cancer is increasingly recognized. Recent research has demonstrated the ability of PCSK9 to modulate immune responses through interactions with immune cells and components of the tumor microenvironment. This includes effects on dendritic cell maturation, T cell activation, and cytokine production, suggesting a role in shaping antitumor immune responses. Moreover, the potential influence of PCSK9 on immune checkpoints such as PD1/PD-L1 lends an additional layer of complexity to its immunomodulatory functions. The growing interest in cancer immunotherapy has prompted exploration into the potential of targeting PCSK9 for therapeutic benefits. Preclinical studies have demonstrated synergistic effects between PCSK9 inhibitors and established immunotherapies, offering a novel avenue for combination treatments. The strategic manipulation of PCSK9 to enhance tumor immunity and improve therapeutic outcomes presents an exciting area for further investigations. Understanding the mechanisms by which PCSK9 influences cancer biology and immunity holds promise for the development of novel immunotherapeutic approaches. This review aims to provide a comprehensive analysis of the intricate connections between PCSK9, cancer pathogenesis, tumor immunity, and the potential implications for immunotherapeutic interventions.

Indexed as

ImmunotherapyNeoplasmsProprotein Convertase 9AnimalsHumansPCSK9 InhibitorsTumor MicroenvironmentPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9Immune checkpointsImmune responsesPCSK9Signaling pathwaysTumor immunity

Identifiers

What Socratic holds

Textmetadata
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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.