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Published in: International Journal of Clinical Oncology 3/2014

01-06-2014 | Original Article

NRAS mutations in primary and metastatic melanomas of Japanese patients

Authors: Hisashi Uhara, Atsuko Ashida, Hiroshi Koga, Eisaku Ogawa, Aya Uchiyama, Ryuhei Uchiyama, Koichi Hayashi, Yukiko Kiniwa, Ryuhei Okuyama

Published in: International Journal of Clinical Oncology | Issue 3/2014

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Abstract

Background

Characterization of the MAPK signaling pathway in melanoma has led to the development of MEK inhibitors for the treatment of NRAS-mutated melanoma. The success of molecular-targeted therapies underscores the need to identify mutations in target genes. Most of the current data on genetic mutations have been obtained from Caucasian melanoma patients, and screenings of Asian populations are limited.

Objective

The aim of the present study was to examine NRAS mutations in primary and metastatic lesions of Japanese melanoma patients.

Methods

Clinical melanoma specimens were collected from 127 Japanese patients, including primary (n = 67), metastatic (n = 25) and paired primary and metastatic lesions (n = 35). NRAS mutations in exons 1 and 2 were assessed by polymerase chain reaction and Sanger sequencing.

Results

The incidence of NRAS mutations was 7.1 %. NRAS Q61 was the predominant genetic alteration (77.8 %). NRAS mutations were most frequently detected in acral melanomas (9.3 %), followed by melanomas without chronic sun-induced damage (7.0 %) and mucosal melanomas (4.8 %), and were not detected in melanomas with chronic sun-induced damage. In addition, NRAS mutations were more prevalent in the extremities than in other sites. The NRAS sequence in metastatic lesions did not match that of the primary tumor in one case.

Conclusion

The frequency of NRAS mutations is lower in the Asian population than in Caucasian patients. The observed heterogeneity of melanoma suggests that genotyping of both primary and metastatic lesions is important to identify candidate patients for molecular-targeted therapies.
Literature
1.
go back to reference Roring M, Brummer T (2012) Aberrant b-raf signaling in human cancer—10 years from bench to bedside. Crit Rev Oncog 17:97–121PubMedCrossRef Roring M, Brummer T (2012) Aberrant b-raf signaling in human cancer—10 years from bench to bedside. Crit Rev Oncog 17:97–121PubMedCrossRef
2.
go back to reference Curtin JA, Fridlyand J, Kageshita T et al (2011) Distinct sets of genetic alterations in melanoma. N Engl J Med 353:2135–2147CrossRef Curtin JA, Fridlyand J, Kageshita T et al (2011) Distinct sets of genetic alterations in melanoma. N Engl J Med 353:2135–2147CrossRef
3.
4.
go back to reference Goel VK, Lazar AJ, Warneke CL et al (2006) Examination of mutations in braf, nras, and pten in primary cutaneous melanoma. J Invest Dermatol 126:154–160PubMedCrossRef Goel VK, Lazar AJ, Warneke CL et al (2006) Examination of mutations in braf, nras, and pten in primary cutaneous melanoma. J Invest Dermatol 126:154–160PubMedCrossRef
5.
6.
go back to reference Lee JH, Choi JW, Kim YS (2011) Frequencies of braf and nras mutations are different in histological types and sites of origin of cutaneous melanoma: a meta-analysis. Br J Dermatol 164:776–784PubMedCrossRef Lee JH, Choi JW, Kim YS (2011) Frequencies of braf and nras mutations are different in histological types and sites of origin of cutaneous melanoma: a meta-analysis. Br J Dermatol 164:776–784PubMedCrossRef
7.
go back to reference Akslen LA, Angelini S, Straume O et al (2005) Braf and nras mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survival. J Invest Dermatol 125:312–317PubMed Akslen LA, Angelini S, Straume O et al (2005) Braf and nras mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survival. J Invest Dermatol 125:312–317PubMed
8.
go back to reference Devitt B, Liu W, Salemi R et al (2011) Clinical outcome and pathological features associated with nras mutation in cutaneous melanoma. Pigment Cell Melanoma Res 24:666–672PubMedCrossRef Devitt B, Liu W, Salemi R et al (2011) Clinical outcome and pathological features associated with nras mutation in cutaneous melanoma. Pigment Cell Melanoma Res 24:666–672PubMedCrossRef
9.
go back to reference Edlundh-Rose E, Egyhazi S, Omholt K et al (2006) Nras and braf mutations in melanoma tumours in relation to clinical characteristics: a study based on mutation screening by pyrosequencing. Melanoma Res 16:471–478PubMedCrossRef Edlundh-Rose E, Egyhazi S, Omholt K et al (2006) Nras and braf mutations in melanoma tumours in relation to clinical characteristics: a study based on mutation screening by pyrosequencing. Melanoma Res 16:471–478PubMedCrossRef
10.
go back to reference Ellerhorst JA, Greene VR, Ekmekcioglu S et al (2011) Clinical correlates of nras and braf mutations in primary human melanoma. Clin Cancer Res 17:229–235PubMedCentralPubMedCrossRef Ellerhorst JA, Greene VR, Ekmekcioglu S et al (2011) Clinical correlates of nras and braf mutations in primary human melanoma. Clin Cancer Res 17:229–235PubMedCentralPubMedCrossRef
11.
go back to reference Si L, Kong Y, Xu X et al (2012) Prevalence of braf v600e mutation in Chinese melanoma patients: large scale analysis of braf and nras mutations in a 432-case cohort. Eur J Cancer 48:94–100PubMedCrossRef Si L, Kong Y, Xu X et al (2012) Prevalence of braf v600e mutation in Chinese melanoma patients: large scale analysis of braf and nras mutations in a 432-case cohort. Eur J Cancer 48:94–100PubMedCrossRef
12.
go back to reference Zhou QM, Li W, Zhang X et al (2012) The mutation profiles of common oncogenes involved in melanoma in southern china. J Invest Dermatol 132:1935–1937PubMedCrossRef Zhou QM, Li W, Zhang X et al (2012) The mutation profiles of common oncogenes involved in melanoma in southern china. J Invest Dermatol 132:1935–1937PubMedCrossRef
13.
go back to reference Ascierto PA, Schadendorf D, Berking C et al (2013) Mek162 for patients with advanced melanoma harbouring nras or val600 braf mutations: a non-randomised, open-label phase 2 study. Lancet Oncol 14:249–256PubMedCrossRef Ascierto PA, Schadendorf D, Berking C et al (2013) Mek162 for patients with advanced melanoma harbouring nras or val600 braf mutations: a non-randomised, open-label phase 2 study. Lancet Oncol 14:249–256PubMedCrossRef
14.
go back to reference Ashida A, Uhara H, Kiniwa Y et al (2012) Assessment of braf and kit mutations in Japanese melanoma patients. J Dermatol Sci 66:240–242PubMedCrossRef Ashida A, Uhara H, Kiniwa Y et al (2012) Assessment of braf and kit mutations in Japanese melanoma patients. J Dermatol Sci 66:240–242PubMedCrossRef
15.
go back to reference Colombino M, Capone M, Lissia A et al (2012) Braf/nras mutation frequencies among primary tumors and metastases in patients with melanoma. J Clin Oncol 30:2522–2529PubMedCrossRef Colombino M, Capone M, Lissia A et al (2012) Braf/nras mutation frequencies among primary tumors and metastases in patients with melanoma. J Clin Oncol 30:2522–2529PubMedCrossRef
16.
go back to reference Falchook GS, Lewis KD, Infante JR et al (2012) Activity of the oral mek inhibitor trametinib in patients with advanced melanoma: a phase 1 dose-escalation trial. Lancet Oncol 13:782–789PubMedCrossRef Falchook GS, Lewis KD, Infante JR et al (2012) Activity of the oral mek inhibitor trametinib in patients with advanced melanoma: a phase 1 dose-escalation trial. Lancet Oncol 13:782–789PubMedCrossRef
17.
go back to reference Kirkwood JM, Bastholt L, Robert C et al (2012) Phase ii, open-label, randomized trial of the mek1/2 inhibitor selumetinib as monotherapy versus temozolomide in patients with advanced melanoma. Clin Cancer Res 18:555–567PubMedCentralPubMedCrossRef Kirkwood JM, Bastholt L, Robert C et al (2012) Phase ii, open-label, randomized trial of the mek1/2 inhibitor selumetinib as monotherapy versus temozolomide in patients with advanced melanoma. Clin Cancer Res 18:555–567PubMedCentralPubMedCrossRef
18.
go back to reference Gerlinger M, Rowan AJ, Horswell S et al (2012) Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med 366:883–892PubMedCrossRef Gerlinger M, Rowan AJ, Horswell S et al (2012) Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med 366:883–892PubMedCrossRef
19.
Metadata
Title
NRAS mutations in primary and metastatic melanomas of Japanese patients
Authors
Hisashi Uhara
Atsuko Ashida
Hiroshi Koga
Eisaku Ogawa
Aya Uchiyama
Ryuhei Uchiyama
Koichi Hayashi
Yukiko Kiniwa
Ryuhei Okuyama
Publication date
01-06-2014
Publisher
Springer Japan
Published in
International Journal of Clinical Oncology / Issue 3/2014
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-013-0573-2

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