scispace - formally typeset
S

Shuang Tang

Researcher at Chinese Academy of Sciences

Publications -  54
Citations -  2471

Shuang Tang is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Herpes simplex virus & Virus. The author has an hindex of 21, co-authored 52 publications receiving 2214 citations. Previous affiliations of Shuang Tang include Center for Biologics Evaluation and Research & Academia Sinica.

Papers
More filters
Journal ArticleDOI

Aberrant expression of oncogenic and tumor-suppressive microRNAs in cervical cancer is required for cancer cell growth.

TL;DR: Analysis of miRNA array analyses for age-matched normal cervix and cervical cancer tissues and cloning and sequencing of a HPV16+ CaSki cell small RNA library indicate that downregulation ofmiR-143 and miR-145 and upregulation ofMiR-146a play a role in cervical carcinogenesis.
Journal ArticleDOI

The E7 Oncoprotein Is Translated from Spliced E6*I Transcripts in High-Risk Human Papillomavirus Type 16- or Type 18-Positive Cervical Cancer Cell Lines via Translation Reinitiation

TL;DR: Direct evidence is provided that the E6*I mRNAs of high-risk HPVs are responsible for E7 production, which was confirmed by transient transfection in 293 cells: E7 could be translated only from the E7 open reading frame (ORF) on E 6*I mRNA in a distance-dependent matter of upstream E6-I ORF by translation reinitiation.
Journal ArticleDOI

An acutely and latently expressed herpes simplex virus 2 viral microRNA inhibits expression of ICP34.5, a viral neurovirulence factor

TL;DR: It is hypothesize that miR-I may modulate the outcome of viral infection in the peripheral nervous system by functioning as a molecular switch for ICP34.5, a key viral neurovirulence factor.
Journal ArticleDOI

Novel less-abundant viral microRNAs encoded by herpes simplex virus 2 latency-associated transcript and their roles in regulating ICP34.5 and ICP0 mRNAs

TL;DR: The use of high-throughput sequencing technology is reported to identify two additional relatively less-abundant viral miRNAs, miR-II andMiR-III, encoded by HSV-2 LAT exon 2.5, which suggest that LAT sequences likely contribute to HSV latency and reactivation through tight control of these LAT-encoded mi RNAs and their viral targets.