Activated leukocyte cell adhesion molecule in breast cancer: prognostic indicator
Creators
- 1. Center for Lung Biology, University of South Alabama, Mobile, Alabama (United States)
- 2. Department of Pharmacology, University of South Alabama, Mobile, Alabama (United States)
- 3. Department of Pathology, University of South Alabama, Mobile, Alabama (United States)
- 4. Department of Cell Biology and Neuroscience, University of South Alabama, Mobile, Alabama (United States)
- 5. Cancer Research Institute, University of South Alabama, Mobile, Alabama (United States)
- 6. Department of Surgery, University of Wales College of Medicine, Cardiff (United Kingdom)
Description
Activated leukocyte cell adhesion molecule (ALCAM) (CD166) is an immunoglobulin molecule that has been implicated in cell migration. The present study examined the expression of ALCAM in human breast cancer and assessed its prognostic value. The immunohistochemical distribution and location of ALCAM was assessed in normal breast tissue and carcinoma. The levels of ALCAM transcripts in frozen tissue (normal breast, n = 32; breast cancer, n = 120) were determined using real-time quantitative PCR. The results were then analyzed in relation to clinical data including the tumor type, the grade, the nodal involvement, distant metastases, the tumor, node, metastasis (TNM) stage, the Nottingham Prognostic Index (NPI), and survival over a 6-year follow-up period. Immunohistochemical staining on tissue sections in ducts/acini in normal breast and in breast carcinoma was ALCAM-positive. Differences in the number of ALCAM transcripts were found in different types of breast cancer. The level of ALCAM transcripts was lower (P = 0.05) in tumors from patients who had metastases to regional lymph nodes compared with those patients without, in higher grade tumors compared with Grade 1 tumors (P < 0.01), and in TNM Stage 3 tumors compared with TNM Stage 1 tumors (P < 0.01). Tumors from patients with poor prognosis (with NPI > 5.4) had significantly lower levels (P = 0.014) of ALCAM transcripts compared with patients with good prognosis (with NPI < 3.4), and tumors from patients with local recurrence had significantly lower levels than those patients without local recurrence or metastases (P = 0.04). Notably, tumors from patients who died of breast cancer had significantly lower levels of ALCAM transcripts (P = 0.0041) than those with primary tumors but no metastatic disease or local recurrence. Patients with low levels of ALCAM transcripts had significantly (P = 0.009) more incidents (metastasis, recurrence, death) compared with patients with primary breast tumors with high levels of ALCAM transcripts. In the present panel of breast cancer specimens, decreased levels of ALCAM correlated with the nodal involvement, the grade, the TNM stage, the NPI, and the clinical outcome (local recurrence and death). The data suggest that decreased ALCAM expression is of clinical significance in breast cancer, and that reduced expression indicates a more aggressive phenotype and poor prognosis
Availability note (English)
Available from http://dx.doi.org/10.1186/bcr815; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC549164Additional details
Identifiers
Publishing Information
- Journal Title
- Breast Cancer Research (Print)
- Journal Volume
- 6
- Journal Issue
- 5
- Journal Page Range
- p. 478-487
- ISSN
- 1465-5411
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47028874
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ADHESION; ANIMAL TISSUES; CARCINOMAS; DEATH; INDICATORS; LEUKOCYTES; LYMPH NODES; MAMMARY GLANDS; METASTASES; MOLECULES; PATIENTS; PLANT TISSUES; POLYMERASE CHAIN REACTION; SOCIO-ECONOMIC FACTORS
- Descriptors DEC
- BIOLOGICAL MATERIALS; BLOOD; BLOOD CELLS; BODY; BODY FLUIDS; DISEASES; GENE AMPLIFICATION; GLANDS; INSTITUTIONAL FACTORS; LYMPHATIC SYSTEM; MATERIALS; NEOPLASMS; ORGANS
Optional Information
- Copyright
- Copyright (c) 2004 King et al.
- Notes
- PMCID: PMC549164; PUBLISHER-ID: bcr815; PMID: 15318930; OAI: oai:pubmedcentral.nih.gov:549164; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.