Research Article - Biomedical Research (2017) Volume 28, Issue 17

Diagnostic values of serum TRACP5b, CEA and CA-153 in predicting bone metastasis in lymph node-negative breast cancer patients

Jing Tang^1#, Juan Liu^2#, Yali Wang², Qingguo Li², Zhengrong Gao², Xiaoming Ma² and Longzhou Chen^2*

¹Department of Urology, Huaian First People's Hospital, Nanjing Medical University, PR China

²Department of Breast Health, Huaian Maternity and Child Healthcare Hospital, Yangzhou University Medical School, PR China

^#These authors contributed equally to this work

*Corresponding Author:

Longzhou Chen
Department of Breast Health
Huaian Maternity and Child Healthcare Hospital
Yangzhou University Medical School, PR China

Accepted date: August 17, 2017

Abstract

Objective: To evaluate the clinical significance of serum levels of Tartrate Resistant Acid Phosphatase 5b (TRACP5b), Carcino-Embryonic Antigen (CEA) and CA-153 in predicting the bone metastasis in patients diagnosed with lymph node-negative breast cancer.

Methods: Seventy-seven patients pathologically diagnosed with lymph node-negative breast cancer were recruited in the breast cancer group and 33 healthy counterparts in the control group. The serum level of TRACP5b was quantitatively measured by Enzyme Linked Immunosorbent Assay (ELISA). The serum levels of CEA and CA-153 were detected by Electrochemiluminescent Immunoassay (ECLIA) and statistically compared between two groups.

Results: In the breast cancer group, the serum levels of TRACP5b, CEA and CA-153 were (3.96 ± 0.87 U/L), (2.67 ± 1.82 ng/ml) and (18.32 ± 7.31 U/ml), significantly up-regulated compared with (2.07 ± 0.83 U/L), (1.36 ± 0.82 ng/ml) and (12.54 ± 7.53 U/ml), respectively (all P<0.05). The sensitivity of serum TRACP5b was 41.56%, significantly higher than 10.39% for CEA and 12.99% for CA-153 (both P<0.05), whereas the specificity of three biomarkers did not significantly differ (all P>0.05). No statistical significance was noted between CEA and CA-153 in terms of sensitivity and specificity (both P>0.05).

Conclusion: Compared with CEA and CA-153, serum TRACP5b yields a higher sensitivity. As one of the serum biomarkers, TRACP5b can be used for the diagnosis of bone metastasis in patients with lymph node-negative breast cancer.

Keywords

Tartrate resistant acid phosphatase 5b, Carcinoembryonic antigen, Carbohydrate antigen-153, Bone metastasis

Introduction

Clinical prognosis of lymph node-breast cancer patients is relatively favorable. Due to the disparity of tumor biomarkers, approximately 30% of lymph node-negative breast cancer patients have a risk of recurrence, metastasis and even death [1]. Bone is the second most common site of metastatic spread in breast cancer and accounts for the highest proportion of first site of relapse in these patients [2]. The annual rate of bone metastases development is higher in node-positive and in estrogen receptor-positive patients [3].

As the disease progresses, almost 70% of patients will develop bone metastases [4]. The median 5 y survival from the diagnosis of bone involvement is 20%, with major causes of morbidity the skeletal related complications, such as pathologic fractures, hypercalcemia and spinal cord compression [5]. Early detection and treatment is of utmost importance, as bone metastasis may influence the quality of patients’ life. At present, detection of serum levels of CEA and CA-153 has been widely used to diagnose the metastasis of breast cancer.

However, the sensitivity of two biomarkers is reported to be relatively low. Plain radiographs remain a conventional method for the diagnosis and follow-up of skeletal involvement while bone scintiography is also used as a whole-body imaging technique with extreme sensitivity. However, advanced-stage bone metastasis can be identified by radiograph examination, which severely affects the clinical outcomes. Tartrate Resistant Acid Phosphatase 5b (TRACP5b), mainly derived from osteoclast, activated macrophages and neurons, has been proven to play a role in reflecting the quantity and function of osteoclasts [6]. It has been hypothesized that TRACP5b is associated with osteoblast migration to bone resorption sites, and TRAP is believed to initiate osteoblast differentiation, activation, and proliferation.

The aim of the present study was to determine the diagnostic validity of serum levels of TRACP5b, CEA and CA-153 in predicting skeletal metastases in patients with lymph nodenegative breast cancer.

Materials and Methods

Baseline characteristics

Seventy-seven breast cancer patients admitted to the Department of Breast Surgery of our hospital between June 2012 and June 2015 were recruited into the breast cancer group. Patients were aged from 29.0 to 73.0 y with a median age of 52.6 y. Among them, 37 cases were premenopausal and 40 were postmenopausal. Prior to surgery, all patients received color ultrasound, CT and MRI examinations. All patients had neither distant metastasis nor lymph node metastasis. They were classified into I-IIa stage breast cancer. Thirty three healthy individuals during breast examination were assigned into the control group including 16 premenopausal and 17 postmenopausal. They were aged from 28 to 57 y with a median age of 46.2 y. No statistical significance was noted between two groups in terms of age and menstruation status, etc. Those with a history of bone fracture, osteoarthritis, rheumatism or osteoporosis in the recent 6 months were excluded from this study. A portion of 3 ml of peripheral blood specimen was collected in the early morning, kept at room temperature for 30 min and centrifuged at 3000 r/min at 4°C for 15 min, restored at -80°C for subsequent analysis within 10 d after sampling collection and preparation.

Informed consents

Written informed consents were obtained from all participants. The study procedures were in accordance with the ethics committee of our hospital.

Equipment and reagents

Elx800 absorbance microplate reader was used for determination of absorbance and concentration of serum cytokines (Bio-Tek, Vermont, USA). The PlGF electrochemiluminescent immunoassays were performed using automated Elecsys 2010 immunoassay analyzer (Roche Diagnostics) strictly according to the manufacturer's instructions. The ELISA reagents and kits were also provided by Roche Corporation.

Detection methods

Prior to ELISA detection, all solutions were restored and balanced at room temperature, and reacted at 18-22°C. The expression level of TRACP5b was quantitatively detected by ELISA strictly according to the manufacturers' instructions. The levels of serum CEA and CA-153 were determined by using electrochemiluminescent immunoassay according to the manufacturers' instructions.

Threshold range

For healthy female subjects, the serum level of TRACP5b should be <4.15 U/L, CA-153<25 U/ml and CEA<4.3 ng/ml. The values exceeding the threshold range are defined as positive outcomes.

Statistical analysis

SPSS 17.0 software package was utilized for statistical analysis in this study (SPSS Inc., Chicago, IL, USA). Measurement data were analysed by independent sample t-test and enumeration data were statistically compared by χ² test. P<0.05 was considered as statistically significant.

Results

Follow-up data

The follow-up endured from 4 to 36 months with a median duration of 24 months. The follow-up rate was calculated as 81.82% (63/77). During follow-up period, one case with bone metastasis and 4 with vertebral metastasis were positive for TRACP5b. One patient with vertebral metastasis was positive for CA-153. The remaining cases had negative outcomes.

Comparison of serum levels of TRACP5b, CA-153 and CEA

Both ELISA and electrochemiluminescence immunoassay demonstrated that the expression levels of TRACP5b, CEA and CA-153 in the breast cancer group were equally significantly higher compared with those in the control group (all P<0.05), as illustrated in Table 1.

Table 1. Comparison of detection values of serum Tracp5b, CEA and CA-153 between two groups.

Comparison of sensitivity and specificity of TRACP5b, CEA and CA-153 detection

As illustrated in Table 2, the sensitivity of TRACP5b detection was calculated as 41.56%, significantly higher compared with 10.39% for CEA and 12.99% for CA-153 (both P<0.05). However, no statistical significance was observed in terms of detection specificity among TRACP5b (100%), CEA (96.97%) and CA-153 (93.94%) (all P>0.05).

Table 2. The diagnostic sensitivity and specificity of TRACP5b, CA-153 and CEA in detection of bone metastasis in patients with breast cancer (%).

Comparison of the scatter tendency of TRACP5b, CEA and CA-153

In the breast cancer group, the median level of serum TRACP5b was calculated as 4.06 U/L and the quartile range was measured from 3.21 to 5.19 U/L. The median concentration of serum CEA was 2.81 ng/ml and the quartile range was between 2.12 and 3.09 ng/ml. The outlier value was detected to be 8.92 ng/ml. The median value of CA-153 level was 18.71 U/ml and the quartile range was between 12.61 and 24.62 U/ml. Two outlier values were 127.8 and 73.1 U/ml. In both groups, the serum levels of TRACP5b remained stable and were found to be normally-distributed. The discrepancy between the TRACP5b level between two groups was insignificant and the scatter tendency of TRACP5b value was significantly less compared with those of CEA and CA-153 (both P<0.05), as illustrated in Figure 1.

Figure 1: Scatter tendency of Tracp5b, CEA and CA-153 in the breast cancer group.

Discussion

In recent years, breast cancer screening has been widely implemented in many countries. Early screening and diagnosis breast cancer is able to significantly enhance the clinical prognosis [7-9]. Film mammography is recommended as the main screening approach, although it has limited sensitivity for the detection of breast cancer in women with radiographically dense breasts. Even though great progression has been achieved due to breast cancer screening, there is still a large quantity of patients with breast cancer metastasis left unidentified [10]. Metastatic bone disease is a frequent cause of morbidity and mortality in patients with advanced breast cancer. Bone metastases can cause severe skeletal morbidity including fractures and hypercalcemia, etc. Tumor cells in the bone are capable of inducing the activation of osteoclasts, which subsequently mediate bone resorption and release of growth factors from bone matrix, leading to a vicious cycle of bone breakdown and tumor proliferation. Wu et al. [11] retrospectively analysed the clinical data of 116 patients with bone metastasis of breast cancer in 20 years and concluded that approximately 63.4% of these breast cancer patients developed bone metastasis within 2 years after surgery. The identification of a highly discriminatory plasma protein profile could provide a tool for the early detection of bone metastasis. Bone metabolic markers are now expected to play a role in the diagnosis and follow-up of bone metastasis. It is recognized that the breast carcinoma affects skeletal metabolism associated with increased bone resorption with or without increased bone formation. The increase bone resorption rate in patients with breast cancer has been indicated significant alterations in an array of serum biomarkers. In this study, early breast cancer patients diagnosed with negative-lymph node were recruited as study subjects. Three serum biomarkers including TRACP5b, CEA and CA-153 were quantitatively measured and statistically compared between the healthy controls and breast cancer counterparts.

Cancer Antigen 15-3 (CA 15-3) and Carcinoembryonic Antigen (CEA), are often used in follow up care of breast cancer and provide important clues to the clinicians for disease progression in metastatic and recurrent breast cancer [12-17]. Triple-negative breast cancers are frequently defined as a single group identifiable using routine clinical tests. Triplenegative breast cancers are defined as negative for estrogen receptor, Progesterone Receptor (PR), and the human epidermal growth factor receptor 2.

Tartrate-Resistant Acid Phosphatase 5b (TRACP 5b) is a specific marker of osteoclasts and is herein proposed as a marker of bone metastasis in breast cancer patients. TRACP 5b activity can be considered a surrogate indicator of bone metastasis in breast cancer patients. Previous studies have demonstrated that serum TRACP5b activity is significantly increased in 70% to 94% of breast cancer patients with bone metastasis. However, the sensitivity and specificity of these serum biomarkers have been rarely studies.

Our findings in this investigation have demonstrated that the serum level of TRACP5b in the breast cancer group is significantly up-regulated compared with that in the healthy controls. More importantly, the sensitivity of TRACP5b detection is equally significantly higher compared with that of CA-153.

In addition, the values of TRACP5b testing remain stable and are found to be normally-distributed. The discrepancy among various detection results is insignificant and the scatter tendency of TRACP5b has been detected to be significantly less than those of CEA and CA-153, suggesting TRACP5b may serve as a novel prognostic factor of breast cancer complicated with bone metastasis. However, the sensitivity and specificity did not significantly differ between CEA and CA-153 testing, indicating that CEA and CA-153 do not differ in terms of the accuracy of prognostic diagnosis of breast carcinoma with bone metastasis. Subsequent follow-up demonstrated that 5 breast cancer patients are found to develop bone metastasis. All these 5 patients are detected to be positive for serum TRACP5b, which is consistent with the findings of Chao et al. [7].

Nevertheless, whether clinical intervention should be delivered for lymph node-negative breast cancer patients with positive TRACP5b remain to be investigated. Moreover, there is no consensus on the diagnostic criterion of TRACP5b, which is able to reflect the osteoclast activity and bone resorption. A reliable diagnostic criterion is urgently required for predicting the clinical prognosis of breast cancer women who are complicated with bone metastasis. The serum level of TRACP5b is influenced by multiple factors, such as age, gender spontaneous or secondary osteopathy, osteoporosis, osteopetrosis, hyperparathyroidism and hyperthyroidism, etc. [8]. A prospective, multi-center investigation with a large sampling size should be carried out to further validate the role of TRACP5b in predicting the clinical prognosis of breast cancer patients with breast cancer.

Acknowledgement

Municipal Key Projects of Applied Research and Science and Technology of Huaian City (Grant.HAS2014012-3).

References

1. Mori M, Mimori K, Inoue H. Detection of cancer metastases in lymPh nodes by reverse transcriptase-polymerase chain reaction. Cancer Res 2005; 55: 3417-3420.
2. Devita VT, Hellman S, Rosenberg SA. Cancer: principles and practice of oncology (7th ed.). Lippincott Williams and Wilkins, Philadelphia 2004; 3120.
3. Smith R, Jiping W, Bryant J, Kay A, Paterson AG, Wolmark N. Primary breast cancer (PBC) as a risk factor for bone recurrence (BR): NSABP experience. Proc Am Soc Clin Oncol 1999; 18: 120.
4. Vincent-Salomon A, Bidard FC, Pierga JY. Bone marrow micrometastasis in breast cancer: Review of detection methods, prognostic impact and biological issues. J Clin Pathol 2008; 61: 570-576.
5. Janckila AJ, Neustadt DH, Nakasato YR. Serum tartrate-resistant acid phosphatase isoforms in rheumatoid arthritis. Clin Chim Acta 2002; 320: 49-58.
6. Capeller B, Caffier H, Sutterlin MW. Evaluation of tartrate-resistant acid phosphatase (TRAP)5b as serum marker of bone metastases in human breast cancer. Anticancer Res 2003; 23: 1011-1015.
7. Chao TY, Yu JC, Ku CH. Tartrate-resistant acid phosphatase 5b is a useful serum marker for extensive bone metastasis in breast cancer Patients. Clin Cancer Res 2005; 11: 544-550.
8. Reichel H, Esser A, Roth HJ. Influence of PTH assay methodology on differential diagnosis of renal bone disease. Nephrol Dial Transplant 2003; 18: 759-768.
9. Fitzgibbons PL, Page DL, Weaver D. Prognostic factors in breast cancer. College of American Pathologists Consensus Statement 1999. Arch Pathol Lab Med 2000; 124: 966-978.
10. McGuckin MA, Cummings MC, Walsh MD. Occult axillary node metastases in breast cancer: their detection and prognostic significance. Br J Cancer 1996; 73: 88-95.
11. Wu J, Shao ZM, Shen KW. Identifying factors related to bone metastasis in breast cancer. China Oncol 2003; 13: 316-318.
12. Chua B, Olivotto IA, Donald JC, Hayashi AH, Doris PJ, Turner L. Outcomes of sentinel lymph node biopsy for breast cancer in British Columbia, 1996 to 2001. Am J Surg 2003; 185: 182-126.
13. Kohlberger P, Gantert M, Volk-Orlowska T, Kieback DG, Gitsch G. Immunohistochemical detection of lymph node metastases in node-negative breast cancer patients. Anticancer Res 2001; 21: 697-699.
14. Colleoni M, Rotmensz N, Peruzzotti G, Maisonneuve P, Mazzarol G, Pruneri G. Size of breast cancer metastases in axillary lymph nodes: Clinical relevance of minimal lymph node involvement. J Clin Oncol 2005; 23: 1379-1389.
15. Cote RJ, Peterson HF, Chaiwun B, Gelber RD, Goldhirsch A, Castiglione-Gertsch M. Role of immunohistochemical detection of lymph-node metastases in management of breast cancer. International Breast Cancer Study Group. Lancet 1999; 354: 896-900.
16. Sakaguchi M, Virmani A, Dudak MW, Peters GN, Leitch AM, Saboorian H. Clinical relevance of reverse transcriptase-polymerase chain reaction for detection of axillary lymph node metastases in breast cancer. Ann Surg Oncol 2003; 10: 117-125.
17. Safai A, Razeghi A, Monabati A, Azarpira N, Talei A. Comparing touch imprint cytology, frozen section analysis, and cytokeratin immunostaining for intraoperative evaluation of axillary sentinel lymph nodes in breast cancer. Ind J Pathol Microbiol 2012; 55: 183-186.