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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Dig Dis Sci. Author manuscript; available in PMC 2010 November 18.
Published in final edited form as:
Dig Dis Sci. 1991 September; 36(9): 1299–1302.
PMCID: PMC2987624
NIHMSID: NIHMS245779

Role of Estrogens and Epidermal Growth Factor in Hepatocellular Carcinoma (HCC)

Abstract

Estrogen (E) and epidermal growth factors (EGF) receptors were assayed in the liver of nine patients with hepatocellular carcinoma (HCC). Total E and nuclear E receptors were decreased significantly in neoplastic tissue as compared to the levels found in surrounding nonneoplastic tissue. The EGF receptor was decreased also in neoplastic tissue. On the basis of binding data, a decrease in the number but not in affinity of both the E and EGF receptors was found.

Keywords: estrogen, epidermal growth factor receptors, hepatocellular carcinoma

Epidermal growth factor (EGF) is a polypeptide growth factor that was isolated originally from the submaxillary gland. It stimulates DNA synthesis in vitro in a variety of different cells (13). This effect is initiated by the interaction of EGF with a specific plasma membrane receptor (4). During the last five years, several lines of evidence have demonstrated that EGF receptor expression can be altered by hormones such as estrogen (E) (4), growth hormone (5), and thyroid stimulating hormone (TSH) (6) in target tissues for these hormones.

The relationship between E and EGF has been studied extensively in normal uterus and in breast cancer tissue (47). For example, it has been shown that E stimulates EGF receptor expression in uterine tissue obtained from immature rats (4). In contrast, an inverse relationship exists between the EGF and E receptors content in breast cancer tissues (8). Recently it has been shown that the liver is also a target tissue for sex hormones (911). E receptors (ER) appear to play an important role in hepatic regeneration where a strong temporal relationship between increased hepatic DNA synthesis and an increased activity and nuclear distribution of ER have been found. Because both ER and EGF are involved in hepatocyte proliferation, the pattern of E and EGF receptors in tissue samples obtained from patients with hepatocellular carcinoma (HCC) was studied.

MATERIALS AND METHODS

Liver Specimens

Samples of HCC-containing and normal adjacent liver were collected from patients undergoing resection in Milan, Bari, and Pittsburgh. Both tumor and adjacent normal liver tissue were collected and their identities confirmed by histology. The samples were wrapped in aluminum foil, snap-frozen, and stored at −70° C until assayed for their content of E and EGF receptors. Prior studies using fresh and frozen liver have showed that both the E and EGF receptors are stable during frozen storage.

Materials

Radioactive [2,3,6,7-3H]estradiol ([3H]E2), 90 Ci/mmol and [125I]EGF were purchased from New England Nuclear. The purity of the radiolabeled compounds was assessed periodically by thin-layer or column chromatography (12). Sources of other materials were as described previously (1214).

Binding Studies

The preparation of cytosolic, nuclear, and plasma membrane fractions was as described previously (10, 15). The methods for the estrogen receptor assay (10) and the EGF binding assay have been described previously (15).

Other Methods

Protein concentrations were determined by the method of Lowry et al (16). DNA concentrations of homogenates and the nuclear preparations were determined by the method of Kissane and Robins (17). Statistical analyses were performed using the Hewlett-Packard 9815S. The radioactivity content of tritiated samples was determined using a Packard TriCarb 4530 with an automatic dpm option. ACS scintillant (Amersham) was used for single-phase counting of tritium-containing samples.

RESULTS

The clinical characteristics of the patients studied have been reported in an earlier paper (18). Figure 1 shows the E receptor activity which was quantitated in both the cytosolic and nuclear fraction as well as in whole tissue. The results are expressed as femtomoles E bound per gram wet liver. The binding capacity of the cytosolic ER was different between nonneoplastic and neoplastic tissue. A trend for an increase in cytosoiic E receptors content in cancerous tissue was evident. The nuclear ER content was significantly lower in neoplastic than in nonneoplastic tissue from the same patient (P < 0.05). Additionally total ER content was reduced in the neoplastic tissue as compared to the nonneoplastic tissue (P < 0.025).

Fig 1
Estrogen receptor activity in HCC (An external file that holds a picture, illustration, etc.
Object name is nihms245779ig2.jpg) and surrounding normal tissues (An external file that holds a picture, illustration, etc.
Object name is nihms245779ig1.jpg). ER activity was measured in cytosoiic (middle panel) and nuclear (lower panel) fractions of HCC and normal liver tissue. Total receptor (top panel) content was calculated by adding ...

Figure 2 shows the EGF binding of plasma membranes isolated from cancerous and surrounding normal hepatic tissue. The values are expressed as femtomoles EGF bound per milligram of membrane protein. It can be seen that hepatic membranes isolated from neoplastic tissue have a lower content of EGF receptor than do membranes isolated from nonneoplastic tissue. The binding affinity data demonstrate that the KD values were similar for normal and neoplastic tissue, demonstrating that the observed reduction in binding is a result of a reduction in number, not affinity, of the receptor.

Fig 2
EGF receptor activity in plasma membranes derived from HCC (An external file that holds a picture, illustration, etc.
Object name is nihms245779ig2.jpg) and normal liver specimens (An external file that holds a picture, illustration, etc.
Object name is nihms245779ig1.jpg).

DISCUSSION

Several lines of evidence have demonstrated a direct relationship between E and EGF receptors. First, the administration of estrogen increases the EGF receptor content in the uterus of immature female rats (4). Second, a similar effect has been reported also in normal breast tissue (7). Recently it has been demonstrated that E may play a role in the regulation of hepatic regeneration in that there is a strong temporal relationship between hepatic DNA synthesis and the nuclear ER content of regenerating liver. In this same model, a reduction in the EGF receptor binding capacity of the liver has been shown to correlate with the increase in EGF receptors. These results have been extended recently in an in vitro model where hepatocytes treated with estrogen have been shown to lose their capacity for EGF-induced stimulation of proliferation (19). These data suggest the existence of a relationship between E receptors, EGF receptors, and tissue growth. Several additional lines of evidence indicate that EGF is involved in proliferation of both normal and neoplastic hepatic tissue. Recently it has become clear that EGF is synthesized at several sites in the body (2022) and that EGF functions more in a paracrine rather than endocrine manner. Considering these facts, it is possible that the regulation of EGF expression in a particular tissue such as the liver might be under endocrine control and help to explain the relationships between TSH and the EGF receptor production in the thyroid, estrogen and the EGF receptor in the uterus, and growth hormone as well as estrogens and the EGF receptor in the liver.

The usual relationship in normal tissue between E and EGF may be altered in neoplastic tissue. In fact, Sainsbury et al (8) recently have reported a significant inverse relationship exists between the activity of the EGF receptor and the E receptor in primary breast cancer tissue. Moreover, EGF receptor was found in tissues with a greater frequency of metastases, presumably having a greater proliferative activity but were E receptor-negative. The results reported here demonstrate that the usual relationship between E receptors and EGF receptors existing in normal tissue is altered in neoplastic hepatic tissue, particularly when there is an overall reduction in the number of EGF receptors (Figure 2).

It is significant that this reduction in EGF receptor content in HCC is proportional to the reduction in ER found in the same tissue and correlates best with a reduction in nuclear E receptor content. It is well known that the nuclear E receptor number is the most biologically important fraction of the total E receptor content of hepatic tissue. The number receptor fraction controls the synthetic activity specific for E (23, 24). In relation to these data it is interesting to note that a reduction in EGF receptor content occurs also in regenerating rat liver but is coupled to an increase in the number of nuclear E receptors. These data demonstrate that in HCC tissue, a reduction in EGF receptor content that is not coupled with an increase in E receptor content occurs. The reasons for and importance of this unusual relationship between E and EGF receptor content in HCC is not known. It may be that, while regenerating rat liver is characterized by rapid proliferation, the growth is tightly regulated and is transient; no permanent growth-controlling alterations in the tissue have occurred and the tissue becomes normal once appropriate growth has concluded. In the case of HCC, the proliferative activity is not regulated by the normal regulatory signals. It is also possible that in neoplastic tissue (25, 26), the EGF receptors are saturated by other growth factors that bind to the receptor such as aipha-TGF, a newly characterized growth substance, which also stimulates cell proliferation via an interaction with the EGF receptor.

Acknowledgments

Supported by the Veterans Administration and Project Grant DK 29961 from the National Institutes of Health, Bethesda, Maryland, and grant 87/01291-44 from Consiglio Nazionale delle Ricerche, Italy.

Footnotes

Presented at the Proceedings of the International Meeting on Normal and Neoplastic Growth in Hepatology, Bari, Italy, June 1989.

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