Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Feb;135(2):191-5.
doi: 10.1007/s00432-008-0458-3. Epub 2008 Aug 29.

Beta-hCG/LH receptor (b-HCG/LH-R) expression is increased in invasive versus preinvasive breast cancer: implications for breast carcinogenesis?

Affiliations

Beta-hCG/LH receptor (b-HCG/LH-R) expression is increased in invasive versus preinvasive breast cancer: implications for breast carcinogenesis?

Gernot Hudelist et al. J Cancer Res Clin Oncol. 2009 Feb.

Abstract

Introduction: The role of the b-HCG/LH/LH-R system in breast cancer is conflicting. Whereas some reports suggest a protective effect of b-HCG on breast epithelium, vitro studies implicate a role of b-HCG/LH-R in the development and growth of breast tumors.

Material and methods: In order to further investigate a possible involvement of b-HCG/LH-R in breast carcinogenesis, immunofluorescence analyses of b-HCG/LH-R expression was performed on 70 preinvasive and adjacent invasive breast cancer specimen using tissue microarrays (TMAs).

Results: In 37 preinvasive samples available for further analysis, b-HCG/LH-R was found in 8/37 samples (21.6%; weak, intermediate and strong staining in 4/37 (10.8%), 2/37 (5.4%) and 2/37 (5.4%). In contrast, b-HCG/LH-R expression was observed in 19/27 (70.4%) adjacent invasive specimen with weak, moderate and strong immunostaining in 10/27 (37.0%), 6/27 (22.2%) and 3/27 (11.1%), respectively. This was statistically significant when compared to preinvasive components (P = 0.001, Chi Square Test).

Conclusions: Based on the observation that b-HCG/LH-R was found to be selectively upregulated in invasive tumor components, we suggest that under certain circumstances, sensitivity of ductal cells to hormones that target b-HCG/LH-R could favour mammary carcinogenesis.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
a, b Immunofluorescence for b-HCG/LH-R lacking receptor expression in ductal components of patients with DCIS (a ×200, b ×400)
Fig. 2
Fig. 2
a, b Immunofluorescence for b-HCG/LH-R exhibiting strong staining intensity in ductal components of patients with DCIS (a ×200, b ×400)
Fig. 3
Fig. 3
a, b Immunofluorescence for b-HCG/LH-R lacking receptor expression in ductal components of patients with adjacent IBC (a ×200, b ×400)
Fig. 4
Fig. 4
a, b Immunofluorescence for b-HCG/LH-R exhibiting strong staining intensity in ductal components of patients with adjacent IBC (a ×200, b ×400)
Fig. 5
Fig. 5
Immunofluorescence for b-HCG/LH-R: absence of specific staining in negative control slide. For primary antibody used see “Materials and methods” (×400)

Similar articles

Cited by

References

    1. Bocker W, Decker T, Ruhnke M, Schneider W (1997) Ductal hyperplasia and ductal carcinoma in situ. Definition–classification–differential diagnosis. Pathologe 18:3–18. doi:10.1007/s002920050191 - PubMed
    1. Dufau ML (1998) The luteinizing hormone receptor. Annu Rev Physiol 60:461–496. doi:10.1146/annurev.physiol.60.1.461 - PubMed
    1. Han SW, Lei ZM, Rao CV (1996) Up-regulation of cyclooxygenase-2 gene expression by chorionic gonadotropin in mucosal cells from human fallopian tubes. Endocrinology 137:2929–2937. doi:10.1210/en.137.7.2929 - PubMed
    1. Hudelist G, Huber A, Knoefler M, et al (2008) Human chorionic gonadotropin/luteinizing hormone receptor (HCG/LH-R) expression in eutopic endometrium and endometriotic implants: evidence for HCG sensitivity of endometriosis. Reprod Sci 15(6):543–551 - PubMed
    1. Kuorelahti A, Rulli S, Huhtaniemi I, Poutanen M (2007) Human chorionic gonadotropin (hCG) up-regulates wnt5b and wnt7b in the mammary gland, and hCGbeta transgenic female mice present with mammary Gland tumors exhibiting characteristics of the Wnt/beta-catenin pathway activation. Endocrinology 148:3694–3703. doi:10.1210/en.2007-0249 - PubMed

Substances