Literature DB >> 28681694

UCHL5 expression associates with improved survival in lymph-node-positive rectal cancer.

Leena Arpalahti1, Jaana Hagström1,2, Harri Mustonen3, Mikael Lundin4, Caj Haglund1,3, Carina I Holmberg1.   

Abstract

Colorectal cancer is among the three most common cancer types for both genders, with a rising global incidence. To date, prognostic evaluation is difficult and largely dependent on early detection and successful surgery. UCHL5/Uch37 is an integral part of the protein homeostasis network as one of the three deubiquitinating enzymes associated with the 26S proteasome. Here, we have investigated in colorectal cancer the possible association of UCHL5 tumor expression and patient survival. UCHL5 tumor expression was evaluated by immunohistochemistry in 779 surgically treated colorectal cancer patients from Helsinki University Hospital, Finland, with assessment of clinicopathological parameters and the effect of UCHL5 expression on patient survival. High and undetectable UCHL5 expression both correlated with increased overall disease-specific survival in the subgroup of patients with lymph-node-positive (Dukes C/stage III) rectal cancer. Within this subgroup of 105 stage-III rectal cancer patients, none of the 7 with high UCHL5 expression died of colorectal cancer within 10 years after surgery ( p = 0.012). A similar, though less prominent, survival trend occurred throughout the whole patient cohort. In conclusion, UCHL5 is a promising novel prognostic marker in lymph-node-positive rectal cancer. Our results also advance the currently limited knowledge of biomarkers in colorectal cancer treatment.

Entities:  

Keywords:  Colorectal cancer; UCHL5; deubiquitination; prognosis; proteasome

Mesh:

Substances:

Year:  2017        PMID: 28681694     DOI: 10.1177/1010428317716078

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  7 in total

1.  Proteasome-associated cysteine deubiquitinases are molecular targets of environmental optical brightener compounds.

Authors:  Isel Castro; Elmira Ekinci; Xuemei Huang; Hassan Ali Cheaito; Young-Hoon Ahn; Jesus Olivero-Verbel; Q Ping Dou
Journal:  J Cell Biochem       Date:  2019-04-08       Impact factor: 4.429

2.  Phosphorylation of Tyr-950 in the proteasome scaffolding protein RPN2 modulates its interaction with the ubiquitin receptor RPN13.

Authors:  Casey W Hemmis; Stephanie C Heard; Christopher P Hill
Journal:  J Biol Chem       Date:  2019-05-07       Impact factor: 5.157

Review 3.  Deubiquitination Reactions on the Proteasome for Proteasome Versatility.

Authors:  Ji Yeong Shin; Srinivasan Muniyappan; Non-Nuoc Tran; Hyeonjeong Park; Sung Bae Lee; Byung-Hoon Lee
Journal:  Int J Mol Sci       Date:  2020-07-27       Impact factor: 5.923

4.  LncRNA DRAIC inhibits proliferation and metastasis of gastric cancer cells through interfering with NFRKB deubiquitination mediated by UCHL5.

Authors:  Zheng Zhang; Xiaoxuan Hu; Jia Kuang; Jinmao Liao; Qi Yuan
Journal:  Cell Mol Biol Lett       Date:  2020-04-25       Impact factor: 5.787

Review 5.  Ubiquitin Carboxyl-Terminal Hydrolases and Human Malignancies: The Novel Prognostic and Therapeutic Implications for Head and Neck Cancer.

Authors:  Chao Rong; Ran Zhou; Shan Wan; Dan Su; Shou-Li Wang; Jochen Hess
Journal:  Front Oncol       Date:  2021-01-29       Impact factor: 6.244

6.  Positive cytoplasmic UCHL5 tumor expression in gastric cancer is linked to improved prognosis.

Authors:  Leena Arpalahti; Alli Laitinen; Jaana Hagström; Harri Mustonen; Arto Kokkola; Camilla Böckelman; Caj Haglund; Carina I Holmberg
Journal:  PLoS One       Date:  2018-02-23       Impact factor: 3.240

7.  The proteasome deubiquitinase inhibitor bAP15 downregulates TGF-β/Smad signaling and induces apoptosis via UCHL5 inhibition in ovarian cancer.

Authors:  Shiho Fukui; Kazunori Nagasaka; Yuko Miyagawa; Ryoko Kikuchi-Koike; Yoshiko Kawata; Ranka Kanda; Takayuki Ichinose; Takeru Sugihara; Haruko Hiraike; Osamu Wada-Hiraike; Yuko Sasajima; Takuya Ayabe
Journal:  Oncotarget       Date:  2019-10-15
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.