To the editor: We read with great interest the recent article ‘MUC4, a novel immunohistochemical marker identified by gene expression profiling, differentiates pleural sarcomatoid mesothelioma from lung sarcomatoid carcinoma’ [1]. Amatya et al found that MUC4 was highly expressed in sarcomatoid lung carcinomas (21/29) and not expressed in sarcomatoid mesotheliomas (0/31), with negative MUC4 expression having a 100% sensitivity and 72% specificity in diagnosing sarcomatoid mesothelioma.
We have attempted to replicate these findings in our own laboratory using the same antibody and staining conditions as reported by Amatya et al. We stained 13 sarcomatoid carcinomas of the lung and 6 sarcomatoid mesotheliomas (Table 1); all of the tumors were confirmed by immunohistochemical staining and imaging/thoracoscopic findings. Of the 13 sarcomatoid carcinomas, 9 showed no staining of the sarcomatoid component at all (Fig. 1), and 3 showed scattered, <1%, positivity in the sarcomatoid component. Only one case showed strong and diffuse positivity in the sarcomatoid component. Most interestingly, three of the sarcomatoid carcinomas also had an epithelial component and the epithelial component stained in all three. All six sarcomatoid mesotheliomas showed no staining. Bronchiolar epithelium that had been overrun by tumor stained strongly and served as a positive internal control (Fig. 1)
In conclusion, although MUC4 may stain sarcomatoid carcinomas of the lung, we found that the frequency/diffuseness of positive staining is too low to make this test useful for separating sarcomatoid carcinomas from sarcomatoid mesotheliomas.
References
Amatya VJ, Kushitani K, Mawas AS, Miyata Y, Okada M, Kishimoto T, Inai K, Takeshima Y. MUC4, a novel immunohistochemical marker identified by gene expression profiling, differentiates pleural sarcomatoid mesothelioma from lung sarcomatoid carcinoma. Mod Pathol. 2017;30:672–81.
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Berg, K.B., Ionescu, D. & Churg, A.M. MUC4 Staining in Sarcomatoid Carcinomas. Mod Pathol 32, 157 (2019). https://doi.org/10.1038/s41379-018-0022-x
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DOI: https://doi.org/10.1038/s41379-018-0022-x