High Expression of Parathyroid Hormone-related Protein and Tumor Necrosis Factor-α in Cancer Cells as Risk Factors for Hypercalcemia in Bone Metastases Lytic Lesions
DOI:
https://doi.org/10.3889/oamjms.2021.5951Keywords:
Bone metastases, Hypercalcemia, Parathyroid hormone-related protein, Tumor necrosis factor-αAbstract
BACKGROUND: Cancer mortality is more commonly due to metastases of the tumor to other organs and the complications that accompany it than the tumor growth itself. Until recently, metastasis has been an insurmountable problem.
AIM: As the most frequent site of metastases, apart from the lungs and liver, tumor metastases to bone are associated with hypercalcemia which is fatal for the affected patient.
METHODS: This study used a case-control study design. The case group consisted of paraffin block samples derived from bone metastatic cancer cell biopsies of patients with hypercalcemic lytic lesions. The control group consisted of paraffin block samples derived from bone metastatic cancer cell biopsies of patients with non-hypercalcemic lytic lesions. Radiological examination was performed to examine the presence of lytic lesions, followed by data collection of serum calcium levels. The data obtained from the histopathological examination was confirmed along with the availability of paraffin blocks of bone metastasis cancer cell biopsy samples, and immunohistochemical analysis was performed to determine the expression of tumor necrosis factor-α _(TNF-α) and parathyroid hormone-related protein (PTHrP). A Mann–Whitney test was performed to determine the expression of TNF-α _and PTHrP between hypercalcemia and non-hypercalcemia groups. To identify the cut-off point, Youden index on receiver operating characteristic was used, then the optimal cut-off point was determined where the sensitivity and specificity curves intersect. Analysis of risk factor assessment was done by creating a 2 × 2 cross-tabulations and calculating the association size in the form of odds ratio (OR).
RESULTS: The expression of PTHrP and TNF-α _in the case group was significantly different from the control group with p < 0.05. The cut-off point for PTHrP expression was 267.5 with an area under the curve of 0.93, indicating a high accuracy value. The cut-off point for TNF-α _expression was 227.5 with an area under the curve of 0.68, indicating a moderate accuracy value. The OR between hypercalcemia and non-hypercalcemia to PTHrP expression was 110.3 (Fisher’s exact statistical test obtained p < 0.05), while the OR between hypercalcemia and non-hypercalcemia to TNF-α _expression was 7.27 (Fisher’s exact test statistical obtained p = 0.01).
CONCLUSION: Significant differences in the expression of PTHrP and TNF-α _were found between patients with bone metastases lytic lesions with hypercalcemia compared to those without hypercalcemia. We can conclude that either a high level of PTHrP expression and/or TNF-α _expression in cancer cells can serve as risk factors for hypercalcemia in patients with bone metastatic lytic lesions.Downloads
Metrics
Plum Analytics Artifact Widget Block
References
Huang JF, Shen J, Li X, Rengan R, Silvestris N, Wang M, et al. Incidence of patients with bone metastases at diagnosis of solid tumors in adults: A large population-based study. Ann Transl Med. 2020;8(7):482. https://doi.org/10.21037/atm.2020.03.55 PMid:32395526 DOI: https://doi.org/10.21037/atm.2020.03.55
Seccareccia D. Palliative care files cancer-related. Can Fam Physician. 2010;56(3):244-6. PMid:20228307
Bollerslev J, Pretorius M, Heck A. Parathyroid hormone independent hypercalcemia in adults. Best Pract Res Clin Endocrinol Metab. 2018;32(5):621-38. https://doi.org/10.1016/j.beem.2018.06.005 PMid:30449545 DOI: https://doi.org/10.1016/j.beem.2018.06.005
Wijaya I, Oehadian A, Sumantri R. Hypercalcemia of malignancy: Clinical characteristics and treatment outcome. Maj Kedokt Bandung. 2014;46(2):111-7. https://doi.org/10.15395/mkb.v46n2.283 DOI: https://doi.org/10.15395/mkb.v46n2.283
Wright LE, Guise TA. The role of PTHrP in skeletal metastases and hypercalcemia of malignancy. Clin Rev Bone Miner Metab. 2014;12(3):119-29. https://doi.org/10.1007/s12018-014-9160-y DOI: https://doi.org/10.1007/s12018-014-9160-y
Clines GA, Guise TA. Hypercalcaemia of malignancy and basic research on mechanisms responsible for osteolytic and osteoblastic metastasis to bone. Endocr Relat Cancer. 2005;12(3):549-83. https://doi.org/10.1677/erc.1.00543 PMid:16172192 DOI: https://doi.org/10.1677/erc.1.00543
Rosner MH, Dalkin AC. Onco-nephrology: The pathophysiology and treatment of malignancy-associated hypercalcemia. Clin J Am Soc Nephrol. 2012;7(10):1722-9. https://doi.org/10.2215/cjn.02470312 PMid:22879438 DOI: https://doi.org/10.2215/CJN.02470312
Montgrain PR, Quintana R, Rascon Y, Burton DW, Deftos LJ, Casillas A, et al. Parathyroid hormone-related protein varies with sex and androgen status in nonsmall cell lung cancer. Cancer. 2007;110(6):1313-20. https://doi.org/10.1002/cncr.22922 PMid:17676588 DOI: https://doi.org/10.1002/cncr.22922
Clines GA. Mechanisms and treatment of hypercalcemia of malignancy. Curr Opin Endocrinol Diabetes Obes. 2011;18(6):339-46. PMid:21897221 DOI: https://doi.org/10.1097/MED.0b013e32834b4401
Pioszak AA, Parker NR, Gardella TJ, Xu HE. Structural basis for parathyroid hormone-related protein binding to the parathyroid hormone receptor and design of conformation-selective peptides. J Biol Chem. 2009;284(41):28382-91. https://doi.org/10.1074/jbc.m109.022905 PMid:19674967 DOI: https://doi.org/10.1074/jbc.M109.022905
Thomas RJ, Guise TA, Yin JJ, Elliott J, Horwood NJ, Martin TJ, et al. Breast cancer cells interact with osteoblasts to support osteoclast formation. Endocrinology. 1999;140(10):4451-8. https://doi.org/10.1210/endo.140.10.7037 PMid:10499498 DOI: https://doi.org/10.1210/endo.140.10.7037
Mundy GR. Metastasis to bone: Causes, consequences and therapeutic opportunities. Nat Rev Cancer. 2002;2(8):584-93. https://doi.org/10.1038/nrc867 PMid:12154351 DOI: https://doi.org/10.1038/nrc867
Boyce BF, Li P, Yao Z, Zhang Q, Badell IR, Schwarz EM, et al. TNF-alpha and pathologic bone resorption. Keio J Med. 2005;54(3):127-31. PMid:16237274 DOI: https://doi.org/10.2302/kjm.54.127
Susanto E. Peran Imunohistokimia p53 Dalam Membedakan Astrositoma Difus Dengan ASstrositosis: Studi Diagnostik; 2014.
Jammal MP, Da Silva AA, Filho AM, Côbo ED, Adad SJ, Murta EF, et al. Immunohistochemical staining of tumor necrosis factor-α _and interleukin-10 in benign and malignant ovarian neoplasms. Oncol Lett. 2015;9(2):979-83. https://doi.org/10.3892/ol.2014.2781 PMid:25624918 DOI: https://doi.org/10.3892/ol.2014.2781
Sufrida N, Hernowo BS, Nur IM, Suryanti S. Parathyroid Hormone-Related Protein (PTHrP) dan Osteonectin (OSN) Sebagai Petunjuk Adanya Penentu Metastasis ke Tulang pada Karsinoma Payudara Duktal Invasif. Vol. 20; 2011.
Wu CE, Wang CW, Huang WK, Yang CT, Wu YC, Hou MM, et al. Cytoplasmic and nuclear parathyroid hormonerelated proteins are opposing prognostic factors in patients with non-small-cell lung cancer who have undergone curative resection. Jpn J Clin Oncol. 2015;45(3):267-73. https://doi.org/10.1093/jjco/hyu202 PMid:25480982 DOI: https://doi.org/10.1093/jjco/hyu202
Dahlan MS. Statistik Untuk Kedokteran Dan Kesehatan. 6th ed. Jakarta: Epidemiologi Indonesia; 2006.
Dahlan MS. Penelitian Diagnostik, Validitas and Reliabilitas. 2nd ed. Jakarta: Epidemiologi Indonesia; 2018.
Chansky, H. A. and Gellman, H. Metastatic Bone Disease. 2020 Available from http://www.emedicine.medscape.com [Last accessed on 2020 Jan 05].
Zacharia B, Subramaniam D, Joy J. Skeletal metastasis an epidemiological study. Indian J Surg Oncol. 2018;9(1):46-51. https://doi.org/10.1007/s13193-017-0706-6 PMid:29563734 DOI: https://doi.org/10.1007/s13193-017-0706-6
Theriault RL, Theriault RL. Biology of bone metastases. Cancer Control. 2012;19(2):92-101. https://doi.org/10.1177/107327481201900203 PMid:22487971 DOI: https://doi.org/10.1177/107327481201900203
Rose PS, Buchowski JM. Metastatic disease in the thoracic and lumbar spine: Evaluation and management. J Am Acad Orthop Surg. 2011;19(1):37-48. PMid:21205766 DOI: https://doi.org/10.5435/00124635-201101000-00005
Maccauro G, Spinelli MS, Mauro S, Perisano C, Graci C, Rosa MA. Physiopathology of Spine Metastasis. Int J Surg Oncol. 2011;2011:107969. https://doi.org/10.1155/2011/107969 PMid:22312491 DOI: https://doi.org/10.1155/2011/107969
Sternlicht H, Glezerman IG. Hypercalcemia of malignancy and new treatment options. Ther Clin Risk Manag. 2015;11:1779-88. https://doi.org/10.2147/tcrm.s83681 PMid:26675713 DOI: https://doi.org/10.2147/TCRM.S83681
Naafs MA. Parathyroid hormone related peptide (PTHrP): A mini-review. Endocrinol Int J. 2017;5(6):321-8. DOI: https://doi.org/10.15406/emij.2017.05.00139
Iddon J, Bundred NJ, Hoyland J, Downey SE, Baird P, Salter D, et al. Expression of parathyroid hormone-related protein and its receptor in bone metastases from prostate cancer. J Pathol. 2000;191(2):170-4. https://doi.org/10.1002/(sici)1096-9896(200006)191:2<170::aid-path620>3.0.co;2- PMid:10861577 DOI: https://doi.org/10.1002/(SICI)1096-9896(200006)191:2<170::AID-PATH620>3.0.CO;2-H
Hayman JA, Danks JA, Martin TJ. Localization of parathyroid hormone-related protein in breast cancer metastases: Increased incidence in bone compared with other sites. Cancer Res. 1991;51(11):3059-61. PMid:2032246
Miki T, Yano S, Hanibuchi M, Kanematsu T, Muguruma H, Sone S. Parathyroid hormone-related protein (PTHRP) is responsible for production of bone metastasis, but not visceral metastasis, by human small cell lung cancer SBC-5 cells in natural killer cell-depleted scid mice. Int J Cancer. 2004;108(4):511-5. https://doi.org/10.1002/ijc.11586 PMid:14696114 DOI: https://doi.org/10.1002/ijc.11586
McDermott MT. Hypercalcemia of malignancy. In: Endocr Secrets. 6th ed. Amsterdam, Netherlands: Elsevier; 2013. p. 142-4. DOI: https://doi.org/10.1016/B978-1-4557-4975-1.00024-3
Vakiti A, Mewawalla P. Malignancy Related Hypercalcemia. In: Pathophysiology. Treasure Island, FL: StatPearls Publishing; 2019. p. 1-4. PMid:11074064
Sethi G, Sung B, Aggarwal B. TNF: A master switch for inflammation to cancer Gautam Sethi, Bokyung Sung, Bharat B. Aggarwal. Front Biosci. 2008;13:5094-107. https://doi.org/10.2741/3066 PMid:18508572 DOI: https://doi.org/10.2741/3066
Hamaguchi T, Wakabayashi H, Matsumine A, Sudo A, Uchida A. TNF inhibitor suppresses bone metastasis in a breast cancer cell line. Biochem Biophys Res Commun. 2011;407(3):525-30. https://doi.org/10.1016/j.bbrc.2011.03.051 PMid:21414299 DOI: https://doi.org/10.1016/j.bbrc.2011.03.051
Yu Y, Ke L, Xia WX, Xiang Y, Lv X, Bu J. Elevated levels of TNF-α _and decreased levels of CD68-positive macrophages in primary tumor tissues are unfavorable for the survival of patients with nasopharyngeal carcinoma. Technol Cancer Res Treat. 2019;18:1-11. https://doi.org/10.1177/1533033819874807 PMid:31522611 DOI: https://doi.org/10.1177/1533033819874807
Mazaki A, Orita S, Inage K, Suzuki M, Abe K, Shiga Y, et al. Tumor necrosis factor-α _produced by osteoclasts might induce intractable pain in a rat spinal metastasis model of breast cancer. Spine Surg Relat Res. 2019;3(3):261-6. https://doi.org/10.22603/ssrr.2018-0106 PMid:31440686 DOI: https://doi.org/10.22603/ssrr.2018-0106
Takahashi S, Hakuta M, Aiba K, Ito Y, Horikoshi N, Miura M, et al. Elevation of circulating plasma cytokines in cancer patients with high plasma parathyroid hormone-related protein levels. Endocr Relat Cancer. 2003;10(3):403-7. https://doi.org/10.1677/erc.0.0100403 PMid:14503917 DOI: https://doi.org/10.1677/erc.0.0100403
Downloads
Published
How to Cite
License
Copyright (c) 2020 Made Wahyu Dharmapradita, I Ketut Suyasa, Made Bramantya Karna, I Wayan Juli Sumadi, Kadek Gede Bakta Giri, Cokorda Krishna Dalem Pemayun, Claudia Santosa (Author)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
http://creativecommons.org/licenses/by-nc/4.0