Widespread expression of parathyroid hormone-related peptide in melanocytic cells

Summary Background Parathyroid hormone‐related peptide (PTH‐rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH‐rP could occur in patients with advanced melanoma. Objectives We examined PTH‐rP expression in cultured melanocytic cell lines and in lesi...

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Published inBritish journal of dermatology (1951) Vol. 148; no. 3; pp. 533 - 538
Main Authors Kageshita, T., Ishihara, T., Tokuo, H., Funasaka, Y., Ichihashi, M., Dong, J., Nakajima, M., Ono, T.
Format Journal Article
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Published Oxford, UK Blackwell Science Ltd 01.03.2003
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Abstract Summary Background Parathyroid hormone‐related peptide (PTH‐rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH‐rP could occur in patients with advanced melanoma. Objectives We examined PTH‐rP expression in cultured melanocytic cell lines and in lesions of melanocytic origin for associations with clinicopathological variables of disease progression. We measured the supernatant and cell lysate level of PTH‐rP in cultured melanoma cells to clarify whether melanoma cells secrete PTH‐rP. Methods PTH‐rP expression was examined by reverse transcriptase–polymerase chain reaction (RT–PCR) in cultured melanocytic cell lines and by immunoperoxidase staining in 18 melanocytic naevi, 40 primary melanoma and 19 metastatic melanoma lesions. The supernatant level of PTH‐rP was measured with an immunoradiometric assay. Results RT–PCR products of PTH‐rP mRNA were detected in six of eight melanoma cell lines; however, neither naevus cells nor melanocytes showed positive products. On the other hand, immunohistochemical analysis showed that PTH‐rP was widely expressed both in benign and malignant melanocytic lesions. In addition, PTH‐rP expression was not associated with any clinicopathological variables. Cell lysate but not the supernatant of melanoma cells showed high PTH‐rP levels. Conclusions These results suggest that PTH‐rP was widely expressed in melanocytic cells; however, the cells did not secrete PTH‐rP.
AbstractList Parathyroid hormone-related peptide (PTH-rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH-rP could occur in patients with advanced melanoma. We examined PTH-rP expression in cultured melanocytic cell lines and in lesions of melanocytic origin for associations with clinicopathological variables of disease progression. We measured the supernatant and cell lysate level of PTH-rP in cultured melanoma cells to clarify whether melanoma cells secrete PTH-rP. PTH-rP expression was examined by reverse transcriptase-polymerase chain reaction (RT-PCR) in cultured melanocytic cell lines and by immunoperoxidase staining in 18 melanocytic naevi, 40 primary melanoma and 19 metastatic melanoma lesions. The supernatant level of PTH-rP was measured with an immunoradiometric assay. RT-PCR products of PTH-rP mRNA were detected in six of eight melanoma cell lines; however, neither naevus cells nor melanocytes showed positive products. On the other hand, immunohistochemical analysis showed that PTH-rP was widely expressed both in benign and malignant melanocytic lesions. In addition, PTH-rP expression was not associated with any clinicopathological variables. Cell lysate but not the supernatant of melanoma cells showed high PTH-rP levels. These results suggest that PTH-rP was widely expressed in melanocytic cells; however, the cells did not secrete PTH-rP.
Summary Background Parathyroid hormone‐related peptide (PTH‐rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH‐rP could occur in patients with advanced melanoma. Objectives We examined PTH‐rP expression in cultured melanocytic cell lines and in lesions of melanocytic origin for associations with clinicopathological variables of disease progression. We measured the supernatant and cell lysate level of PTH‐rP in cultured melanoma cells to clarify whether melanoma cells secrete PTH‐rP. Methods PTH‐rP expression was examined by reverse transcriptase–polymerase chain reaction (RT–PCR) in cultured melanocytic cell lines and by immunoperoxidase staining in 18 melanocytic naevi, 40 primary melanoma and 19 metastatic melanoma lesions. The supernatant level of PTH‐rP was measured with an immunoradiometric assay. Results RT–PCR products of PTH‐rP mRNA were detected in six of eight melanoma cell lines; however, neither naevus cells nor melanocytes showed positive products. On the other hand, immunohistochemical analysis showed that PTH‐rP was widely expressed both in benign and malignant melanocytic lesions. In addition, PTH‐rP expression was not associated with any clinicopathological variables. Cell lysate but not the supernatant of melanoma cells showed high PTH‐rP levels. Conclusions These results suggest that PTH‐rP was widely expressed in melanocytic cells; however, the cells did not secrete PTH‐rP.
BACKGROUNDParathyroid hormone-related peptide (PTH-rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH-rP could occur in patients with advanced melanoma.OBJECTIVESWe examined PTH-rP expression in cultured melanocytic cell lines and in lesions of melanocytic origin for associations with clinicopathological variables of disease progression. We measured the supernatant and cell lysate level of PTH-rP in cultured melanoma cells to clarify whether melanoma cells secrete PTH-rP.METHODSPTH-rP expression was examined by reverse transcriptase-polymerase chain reaction (RT-PCR) in cultured melanocytic cell lines and by immunoperoxidase staining in 18 melanocytic naevi, 40 primary melanoma and 19 metastatic melanoma lesions. The supernatant level of PTH-rP was measured with an immunoradiometric assay.RESULTSRT-PCR products of PTH-rP mRNA were detected in six of eight melanoma cell lines; however, neither naevus cells nor melanocytes showed positive products. On the other hand, immunohistochemical analysis showed that PTH-rP was widely expressed both in benign and malignant melanocytic lesions. In addition, PTH-rP expression was not associated with any clinicopathological variables. Cell lysate but not the supernatant of melanoma cells showed high PTH-rP levels.CONCLUSIONSThese results suggest that PTH-rP was widely expressed in melanocytic cells; however, the cells did not secrete PTH-rP.
Author Ichihashi, M.
Funasaka, Y.
Dong, J.
Ishihara, T.
Ono, T.
Tokuo, H.
Kageshita, T.
Nakajima, M.
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Keywords Human
Cell culture
parathyroid hormone-related peptide
Melanocyte
Malignant melanoma
Parathyroid hormone related peptide
disease progression
Language English
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Snippet Summary Background Parathyroid hormone‐related peptide (PTH‐rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of...
Parathyroid hormone-related peptide (PTH-rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH-rP could occur...
BACKGROUNDParathyroid hormone-related peptide (PTH-rP) was associated with the syndrome of hypercalcaemia of malignancy. An increased serum level of PTH-rP...
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StartPage 533
SubjectTerms Adolescent
Adult
Aged
Aged, 80 and over
Biological and medical sciences
Child
Dermatology
disease progression
Female
Humans
Immunohistochemistry - methods
Investigative techniques, diagnostic techniques (general aspects)
Male
malignant melanoma
Medical sciences
Melanocytes - metabolism
Melanoma - metabolism
Middle Aged
Nevus - metabolism
parathyroid hormone-related peptide
Parathyroid Hormone-Related Protein
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Peptide Hormones - analysis
Peptide Hormones - blood
Reverse Transcriptase Polymerase Chain Reaction - methods
RNA, Messenger - analysis
Skin Neoplasms - metabolism
Tumor Cells, Cultured
Title Widespread expression of parathyroid hormone-related peptide in melanocytic cells
URI https://api.istex.fr/ark:/67375/WNG-ZKNJ4DPT-S/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1046%2Fj.1365-2133.2003.05171.x
https://www.ncbi.nlm.nih.gov/pubmed/12653746
https://www.proquest.com/docview/200091273/abstract/
https://search.proquest.com/docview/73125484
Volume 148
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