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DOI 10.1007/s11102-021-01151-6

Медицинская библиотека · Pituitary · 2021

Identification of mutant K-RAS in pituitary macroadenoma.

Aran Veronica, Heringer Manoela, da Mata Paulo Jose, Kasuki Leandro, Miranda Renan Lyra, Andreiuolo Felipe, Chimelli Leila, Filho Paulo Niemeyer, Gadelha Monica Roberto, Neto Vivaldo Moura

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Аннотация

PURPOSE: RAS genes are among the most frequently mutated genes in cancer, where their mutation frequency varies according to the distinct RAS isoforms and tumour types. Despite occurring more prevalent in malignant tumours, RAS mutations were also observed in few benign tumours. Pituitary adenomas are examples of benign tumours which vary in size and aggressiveness. The present study was performed to investigate, via liquid biopsy and tissue analysis, the presence of K-RAS mutations in a pituitary macroadenoma.

METHODS

Molecular analysis was performed to investigate K-RAS mutations using the droplet digital PCR (ddPCR) method by evaluating both plasma (liquid biopsy) and the solid tumour of a patient diagnosed with a giant clinically non-functioning pituitary tumour.

RESULTS

The patient underwent surgical resection due to visual loss, and the histopathological analysis showed a gonadotrophic pituitary macroadenoma. The molecular analysis revealed the presence of mutant K-RAS both in the plasma and in the tumour tissue which, to our knowledge, has not been previously reported in the literature.

CONCLUSION

Our findings highlight the exceptional capacity of the digital PCR in detecting low frequency mutations (below 1%), since we detected, for the first time, K-RAS mutations in pituitary macroadenoma. The potential impact of K-RAS mutations in these tumours should be further investigated.

Для цитирования: Aran Veronica, Heringer Manoela, da Mata Paulo Jose, Kasuki Leandro, Miranda Renan Lyra, Andreiuolo Felipe, Chimelli Leila, Filho Paulo Niemeyer, Gadelha Monica Roberto, Neto Vivaldo Moura. Identification of mutant K-RAS in pituitary macroadenoma.. Pituitary. 2021. DOI: 10.1007/s11102-021-01151-6.

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