Abstract

Simple SummaryKaposi’s sarcoma-associated herpesvirus (KSHV) is one of the seven oncogenic viruses currently recognized by the International Agency for Research on Cancer. Its presence for Kaposi’s sarcoma development is essential and knowledge on the oncogenic process has increased since its discovery in 1994. However, some uncertainties remain to be clarified, in particular on the exact routes of transmission and disparities in KSHV seroprevalence and the prevalence of Kaposi’s sarcoma worldwide. Here, we summarized the current data on the KSHV viral particle’s structure, its genome, the replication, its seroprevalence, the viral diversity and the lytic and latent oncogenesis proteins involved in Kaposi’s sarcoma. Lastly, we reported the environmental, immunological and viral factors possibly associated with KSHV transmission that could also play a role in the development of Kaposi’s sarcoma.Kaposi’s sarcoma-associated herpesvirus (KSHV), also called human herpesvirus 8 (HHV-8), is an oncogenic virus belonging to the Herpesviridae family. The viral particle is composed of a double-stranded DNA harboring 90 open reading frames, incorporated in an icosahedral capsid and enveloped. The viral cycle is divided in the following two states: a short lytic phase, and a latency phase that leads to a persistent infection in target cells and the expression of a small number of genes, including LANA-1, v-FLIP and v-cyclin. The seroprevalence and risk factors of infection differ around the world, and saliva seems to play a major role in viral transmission. KSHV is found in all epidemiological forms of Kaposi’s sarcoma including classic, endemic, iatrogenic, epidemic and non-epidemic forms. In a Kaposi’s sarcoma lesion, KSHV is mainly in a latent state; however, a small proportion of viral particles (<5%) are in a replicative state and are reported to be potentially involved in the proliferation of neighboring cells, suggesting they have crucial roles in the process of tumorigenesis. KSHV encodes oncogenic proteins (LANA-1, v-FLIP, v-cyclin, v-GPCR, v-IL6, v-CCL, v-MIP, v-IRF, etc.) that can modulate cellular pathways in order to induce the characteristics found in all cancer, including the inhibition of apoptosis, cells’ proliferation stimulation, angiogenesis, inflammation and immune escape, and, therefore, are involved in the development of Kaposi’s sarcoma.

Highlights

  • Kaposi’s sarcoma-associated herpesvirus (KSHV), called human herpesvirus 8 (HHV-8), is an oncogenic virus belonging to the Herpesviridae family

  • KSHV encodes oncogenic proteins (LANA-1, v-FLIP, v-cyclin, v-GPCR, v-IL6, v-CCL, v-MIP, v-IRF, etc.) that can modulate cellular pathways in order to induce the characteristics found in all cancer, including the inhibition of apoptosis, cells’ proliferation stimulation, angiogenesis, inflammation and immune escape, and, are involved in the development of Kaposi’s sarcoma

  • Epidemiological and molecular studies have subsequently confirmed the association between KSHV and Kaposi’s sarcoma, and it became one of the ten carcinogenic infectious agents in humans listed by the International Agency for Research on Cancer (IARC)

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Summary

Introduction

(HHV-8), is an oncogenic virus that was discovered in 1994 by Chang et al in the USA [1]. They described, for the first time, two viral fragments of 330 and 631 base pairs (bp) in skin biopsies issued from AIDS patients with Kaposi’s sarcoma (KS). These fragments, identified through a representational difference analysis assay, were phylogenetically closed to the Epstein–Barr virus (EBV), and to the saimiri herpesvirus (Saimirine herpesvirus 2, SaHV-2). Epidemiological and molecular studies have subsequently confirmed the association between KSHV and Kaposi’s sarcoma, and it became one of the ten carcinogenic infectious agents in humans listed by the International Agency for Research on Cancer (IARC) (https://monographs.iarc.who.int/list-of-classifications, accessed on 4 December 2021.)

Classification
Viral Genome
Entry in the Cell
KSHV Latent Cycle
KSHV Lytic Cycle
Transmission in Countries with Low Seroprevalence
Transmission in Endemic Regions
Molecular Epidemiology
ORF-K1
Molecular Diversity and Pathogenicity
KSHV Latency Proteins and Oncogenesis
Lytic Proteins and Oncogenesis
Rationale and Feasibility of KSHV Vaccine
Findings
Conclusions

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