Molecular mechanisms of arsenic carcinogenesis

C Huang, Q Ke, M Costa, X Shi - Molecular and cellular biochemistry, 2004 - Springer
Arsenic is a metalloid compound that is widely distributed in the environment. Human
exposure of this compound has been associated with increased cancer incidence. Although …

The paradox of arsenic: molecular mechanisms of cell transformation and chemotherapeutic effects

AM Bode, Z Dong - Critical reviews in oncology/hematology, 2002 - Elsevier
Arsenic is a well-documented carcinogen that also appears to be a valuable therapeutic tool
in cancer treatment. This creates a paradox for which no unified hypothesis has been …

A novel function of the MA-3 domains in transformation and translation suppressor Pdcd4 is essential for its binding to eukaryotic translation initiation factor 4A

HS Yang, MH Cho, H Zakowicz… - … and cellular biology, 2004 - Taylor & Francis
Αn α-helical MA-3 domain appears in several translation initiation factors, including human
eukaryotic translation initiation factor 4G (eIF4G) and DAP-5/NAT1/p97, as well as in the …

Inhibition of Activator Protein 1 Activity and Cell Growth by Purified Green Tea and Black Tea Polyphenols in H-ras-transformed Cells: Structure-Activity Relationship …

JY Chung, C Huang, X Meng, Z Dong, CS Yang - Cancer Research, 1999 - AACR
Abstract ras gene mutation, which perpetually turns on the growth signal transduction
pathway, occurs frequently in many cancer types. The mouse epidermal JB6 cell line has …

Blocking activator protein-1 activity, but not activating retinoic acid response element, is required for the antitumor promotion effect of retinoic acid

C Huang, WY Ma, MI Dawson… - Proceedings of the …, 1997 - National Acad Sciences
Retinoic acid is one of the most promising drugs for chemotherapy and chemoprevention of
cancer. Either blocking activator protein-1 (AP-1) activity or activating retinoic acid response …

Suppression of Skin Tumorigenesis in c-Jun NH2-Terminal Kinase-2-Deficient Mice

N Chen, M Nomura, QB She, WY Ma, AM Bode… - Cancer research, 2001 - AACR
Previous studies have shown that c-Jun NH2-terminal kinase (JNK) belongs to the mitogen-
activated protein kinase (MAPK) family of signal transduction components that are rapidly …

Clinical significance of long intergenic noncoding RNA-p21 in colorectal cancer

H Zhai, A Fesler, K Schee, Ø Fodstad, K Flatmark… - Clinical colorectal …, 2013 - Elsevier
Abstract Background Long intergenic noncoding RNAs (lincRNAs) have been shown to be
novel regulators for both transcription and posttranscriptional/translation. One of them …

LincRNa-p21: function and mechanism in cancer

S Chen, H Liang, H Yang, K Zhou, L Xu, J Liu, B Lai… - Medical Oncology, 2017 - Springer
In view of the rapid development of gene chips and high-throughput sequencing technology,
noncoding RNAs (ncRNas) form a high percentage of the mammalian genome. Two major …

Pdcd4 suppresses tumor phenotype in JB6 cells by inhibiting AP-1 transactivation

HS Yang, JL Knies, C Stark, NH Colburn - Oncogene, 2003 - nature.com
Transformation suppressor Pdcd4 is downregulated in transformed (Tx) mouse epidermal
JB6 RT101 cells relative to transformation-resistant (P−) and susceptible (P+) variants …

Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced NF-κB activation by tea polyphenols, (–)-epigallocatechin gallate and theaflavins

M Nomura, W Ma, N Chen, AM Bode, Z Dong - Carcinogenesis, 2000 - academic.oup.com
(–)-Epigallocatechin gallate (EGCG) and theaflavins are believed to be the key active
components in tea for the chemoprevention of cancer. However, the molecular mechanisms …