Evidence map›Paper›PMID 35626397›Full record

ReviewDiagnostics (Basel, Switzerland)2022

Kaposi Sarcoma, a Trifecta of Pathogenic Mechanisms.

Gabriela Rusu-Zota, Oana Mădălina Manole, Cristina Galeș, Elena Porumb-Andrese, Otilia Obadă, Cezar Valentin Mocanu

Open access · goldAbstract readReview
In one paragraph

Review in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 21 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 1 institution in 1 country.

Gabriela Rusu-ZotaDepartment of Pharmacology, Clinical Pharmacology and Algesiology, Faculty of Medicine, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, 700115 Iasi, Romania.
Oana Mădălina ManoleFaculty of Medicine, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, 700115 Iasi, Romania.
Cristina GaleșDepartment of Histology, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, 700115 Iasi, Romania.
Elena Porumb-AndreseDepartment of Dermatology, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, 700115 Iasi, Romania.ORCID 0000-0002-2859-2066
Otilia ObadăDepartment of Ophthalmology, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, 700115 Iasi, Romania.ORCID 0000-0003-2593-0135
Cezar Valentin MocanuDepartment of Anatomical Pathology, University of Medicine and Pharmacy "Grigore T. Popa" Iasi, 700115 Iasi, Romania.
Grigore T. Popa University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kaposi's sarcoma is a rare disease with four known variants: classic, epidemic, endemic and iatrogenic (transplant-related), all caused by an oncogenic virus named Human Herpes Virus 8. The viral infection in itself, along with the oncogenic properties of HHV8 and with immune system dysfunction, forms the grounds on which Kaposi's Sarcoma may develop. Infection with HHV8 occurs through saliva via close contacts, blood, blood products, solid organ donation and, rarely, vertical transmission. Chronic inflammation and oncogenesis are promoted by a mix of viral genes that directly promote cell survival and transformation or interfere with the regular cell cycle and cell signaling (of particular note: LANA-1, v-IL6, vBCL-2, vIAP, vIRF3, vGPCR, gB, K1, K8.1, K15). The most common development sites for Kaposi's sarcoma are the skin, mucocutaneous zones, lymph nodes and visceral organs, but it can also rarely appear in the musculoskeletal system, urinary system, endocrine organs, heart or eye. Histopathologically, spindle cell proliferation with slit-like vascular spaces, plasma cell and lymphocyte infiltrate are characteristic. The clinical presentation is heterogenic depending on the variant; some patients have indolent disease and others have aggressive disease. The treatment options include highly active antiretroviral therapy, surgery, radiation therapy, chemotherapy, and immunotherapy. A literature search was carried out using the MEDLINE/PubMed, SCOPUS and Google Scholar databases with a combination of keywords with the aim to provide critical, concise, and comprehensive insights into advances in the pathogenic mechanism of Kaposi's sarcoma.

Indexed as

angiogenesishuman herpes virus 8immune modulationimmunosuppressionKaposi’s sarcomaoncogenesisskin cancer

Identifiers

PMID35626397
PMCPMC9140574
OpenAlexW4280579059

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.