Frequent activating HRAS mutations in trichilemmoma

J. H. Tsai, W. C. Huang, J. Y. Jhuang, Y. M. Jeng, M. L. Cheng, H. Y. Chiu, K. T. Kuo, J. Y. Liau

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Summary Background Trichilemmoma is a benign follicular epithelial tumour exhibiting outer root sheath differentiation. It is associated with Cowden syndrome and naevus sebaceus (NS), but the pathogenesis of sporadic tumours is poorly understood. Recently, NS was found to be caused by postzygotic HRAS or KRAS mutations.

Objectives We sought to determine whether NS-related and NS-unrelated trichilemmomas harbour RAS mutations.

Methods Formalin-fixed and paraffin-embedded blocks of 12 NS-related and 15 NS-unrelated trichilemmomas from 26 individuals were retrieved and analysed to determine the presence of mutations in exons 1 and 2 of the HRAS, KRAS and NRAS genes by polymerase chain reaction and direct sequencing. Mutational hotspots of the FGFR3 and PIK3CA genes were also analysed for NS-unrelated cases.

Results Among the 27 cases, mutually exclusive HRAS c.37G>C and c.182A>G mutations were observed in 17 and three tumours, respectively. Of the 12 NS-related tumours, 11 (92%) harboured the HRAS c.37G>C substitution. Of the 15 sporadic tumours, nine (60%) harboured HRAS mutations, including six c.37G>C and three c.182A>G. An HRAS c.182A>G mutation was observed only in sporadic tumours. No mutations were observed in the other genes that were tested.

Conclusions The high frequency of HRAS activating mutations, including the c.182A>G substitution, which was rather rare in NS, suggests that most trichilemmomas are authentic neoplasms. What's already known about this topic? Virtually all cases of naevus sebaceus (NS) are caused by postzygotic HRAS or KRAS mutations. Trichilemmoma is among the most common secondary tumours associated with NS. What does this study add? Sporadic trichilemmomas frequently harbour activating HRAS mutations, including the c.182A>G substitution, which is rather rare in NS. The high frequency of activating HRAS mutations suggests that most trichilemmomas are authentic neoplasms.

Original languageEnglish
Pages (from-to)1073-1077
Number of pages5
JournalBritish Journal of Dermatology
Volume171
Issue number5
DOIs
Publication statusPublished - Jan 1 2014

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Nevus
Mutation
Neoplasms
Multiple Hamartoma Syndrome
Genes
Paraffin
Formaldehyde
Exons

ASJC Scopus subject areas

  • Dermatology

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Frequent activating HRAS mutations in trichilemmoma. / Tsai, J. H.; Huang, W. C.; Jhuang, J. Y.; Jeng, Y. M.; Cheng, M. L.; Chiu, H. Y.; Kuo, K. T.; Liau, J. Y.

In: British Journal of Dermatology, Vol. 171, No. 5, 01.01.2014, p. 1073-1077.

Research output: Contribution to journalArticle

Tsai, J. H. ; Huang, W. C. ; Jhuang, J. Y. ; Jeng, Y. M. ; Cheng, M. L. ; Chiu, H. Y. ; Kuo, K. T. ; Liau, J. Y. / Frequent activating HRAS mutations in trichilemmoma. In: British Journal of Dermatology. 2014 ; Vol. 171, No. 5. pp. 1073-1077.
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abstract = "Summary Background Trichilemmoma is a benign follicular epithelial tumour exhibiting outer root sheath differentiation. It is associated with Cowden syndrome and naevus sebaceus (NS), but the pathogenesis of sporadic tumours is poorly understood. Recently, NS was found to be caused by postzygotic HRAS or KRAS mutations.Objectives We sought to determine whether NS-related and NS-unrelated trichilemmomas harbour RAS mutations.Methods Formalin-fixed and paraffin-embedded blocks of 12 NS-related and 15 NS-unrelated trichilemmomas from 26 individuals were retrieved and analysed to determine the presence of mutations in exons 1 and 2 of the HRAS, KRAS and NRAS genes by polymerase chain reaction and direct sequencing. Mutational hotspots of the FGFR3 and PIK3CA genes were also analysed for NS-unrelated cases.Results Among the 27 cases, mutually exclusive HRAS c.37G>C and c.182A>G mutations were observed in 17 and three tumours, respectively. Of the 12 NS-related tumours, 11 (92{\%}) harboured the HRAS c.37G>C substitution. Of the 15 sporadic tumours, nine (60{\%}) harboured HRAS mutations, including six c.37G>C and three c.182A>G. An HRAS c.182A>G mutation was observed only in sporadic tumours. No mutations were observed in the other genes that were tested.Conclusions The high frequency of HRAS activating mutations, including the c.182A>G substitution, which was rather rare in NS, suggests that most trichilemmomas are authentic neoplasms. What's already known about this topic? Virtually all cases of naevus sebaceus (NS) are caused by postzygotic HRAS or KRAS mutations. Trichilemmoma is among the most common secondary tumours associated with NS. What does this study add? Sporadic trichilemmomas frequently harbour activating HRAS mutations, including the c.182A>G substitution, which is rather rare in NS. The high frequency of activating HRAS mutations suggests that most trichilemmomas are authentic neoplasms.",
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AU - Tsai, J. H.

AU - Huang, W. C.

AU - Jhuang, J. Y.

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AU - Cheng, M. L.

AU - Chiu, H. Y.

AU - Kuo, K. T.

AU - Liau, J. Y.

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N2 - Summary Background Trichilemmoma is a benign follicular epithelial tumour exhibiting outer root sheath differentiation. It is associated with Cowden syndrome and naevus sebaceus (NS), but the pathogenesis of sporadic tumours is poorly understood. Recently, NS was found to be caused by postzygotic HRAS or KRAS mutations.Objectives We sought to determine whether NS-related and NS-unrelated trichilemmomas harbour RAS mutations.Methods Formalin-fixed and paraffin-embedded blocks of 12 NS-related and 15 NS-unrelated trichilemmomas from 26 individuals were retrieved and analysed to determine the presence of mutations in exons 1 and 2 of the HRAS, KRAS and NRAS genes by polymerase chain reaction and direct sequencing. Mutational hotspots of the FGFR3 and PIK3CA genes were also analysed for NS-unrelated cases.Results Among the 27 cases, mutually exclusive HRAS c.37G>C and c.182A>G mutations were observed in 17 and three tumours, respectively. Of the 12 NS-related tumours, 11 (92%) harboured the HRAS c.37G>C substitution. Of the 15 sporadic tumours, nine (60%) harboured HRAS mutations, including six c.37G>C and three c.182A>G. An HRAS c.182A>G mutation was observed only in sporadic tumours. No mutations were observed in the other genes that were tested.Conclusions The high frequency of HRAS activating mutations, including the c.182A>G substitution, which was rather rare in NS, suggests that most trichilemmomas are authentic neoplasms. What's already known about this topic? Virtually all cases of naevus sebaceus (NS) are caused by postzygotic HRAS or KRAS mutations. Trichilemmoma is among the most common secondary tumours associated with NS. What does this study add? Sporadic trichilemmomas frequently harbour activating HRAS mutations, including the c.182A>G substitution, which is rather rare in NS. The high frequency of activating HRAS mutations suggests that most trichilemmomas are authentic neoplasms.

AB - Summary Background Trichilemmoma is a benign follicular epithelial tumour exhibiting outer root sheath differentiation. It is associated with Cowden syndrome and naevus sebaceus (NS), but the pathogenesis of sporadic tumours is poorly understood. Recently, NS was found to be caused by postzygotic HRAS or KRAS mutations.Objectives We sought to determine whether NS-related and NS-unrelated trichilemmomas harbour RAS mutations.Methods Formalin-fixed and paraffin-embedded blocks of 12 NS-related and 15 NS-unrelated trichilemmomas from 26 individuals were retrieved and analysed to determine the presence of mutations in exons 1 and 2 of the HRAS, KRAS and NRAS genes by polymerase chain reaction and direct sequencing. Mutational hotspots of the FGFR3 and PIK3CA genes were also analysed for NS-unrelated cases.Results Among the 27 cases, mutually exclusive HRAS c.37G>C and c.182A>G mutations were observed in 17 and three tumours, respectively. Of the 12 NS-related tumours, 11 (92%) harboured the HRAS c.37G>C substitution. Of the 15 sporadic tumours, nine (60%) harboured HRAS mutations, including six c.37G>C and three c.182A>G. An HRAS c.182A>G mutation was observed only in sporadic tumours. No mutations were observed in the other genes that were tested.Conclusions The high frequency of HRAS activating mutations, including the c.182A>G substitution, which was rather rare in NS, suggests that most trichilemmomas are authentic neoplasms. What's already known about this topic? Virtually all cases of naevus sebaceus (NS) are caused by postzygotic HRAS or KRAS mutations. Trichilemmoma is among the most common secondary tumours associated with NS. What does this study add? Sporadic trichilemmomas frequently harbour activating HRAS mutations, including the c.182A>G substitution, which is rather rare in NS. The high frequency of activating HRAS mutations suggests that most trichilemmomas are authentic neoplasms.

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