4.2 Article

Abnormal accumulation of human transmembrane (TMEM)-176A and 176B proteins is associated with cancer pathology

Journal

ACTA HISTOCHEMICA
Volume 114, Issue 7, Pages 705-712

Publisher

ELSEVIER GMBH, URBAN & FISCHER VERLAG
DOI: 10.1016/j.acthis.2011.12.006

Keywords

Breast cancer; Melanoma; Lymphoma; Hepatocellular carcinoma

Categories

Funding

  1. NSF [MCB 920127]
  2. NIH [R15-NS070774]
  3. HHMI Undergraduate Research Program
  4. CSUF Office of Grants and Contracts
  5. Direct For Biological Sciences
  6. Div Of Molecular and Cellular Bioscience [0920127] Funding Source: National Science Foundation

Ask authors/readers for more resources

Transmembrane (TMEM)-176A and 176B proteins belong to the MS4A family of proteins whose function in the immune system remains unclear. TMEM176A transcripts were previously shown to be elevated in liver cancer or kidney tissue with proteinuria, while marked changes in TMEM176B transcripts have been found in tolerated tissue allografts and neoplastic fibroblasts. To study the functional relationship between human TMEM176A and 176B and their putative link to cancer, we used polymerase chain reaction and biochemical assays. Here, we show that TMEM176A and 1768 are widely expressed in all human tissues examined. Co-immunoprecipitation of heterologously expressed TMEM176A and 176B revealed direct physical interaction. To determine the relevance of such interaction to cancer pathology, we analyzed biopsied tissue samples from a variety of normal and cancer tissues. Our data reveal that human TMEM176A and 176B protein levels are significantly elevated in lymphoma, but not in normal tissues. The protein levels of TMEM176A are also significantly increased in lung carcinoma. Finally, analysis of the protein expression ratio of TMEM176A over 1768 showed significant differences between normal and cancer tissues of the breast, lymph, skin, and liver, which indicates that both TMEM proteins could be potential useful markers for certain human cancers. (c) 2011 Elsevier GmbH. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available