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Correction to: Methylation of ZNF331 is an independent prognostic marker of colorectal cancer and promotes colorectal cancer growth

The Original Article was published on 18 October 2017

Correction

After publication of the original article [1], it came to the authors’ attention that a reference was omitted from the Background. The reference should have been inserted as [16] and is the following:

Vedeld HM, Andresen K, Eilertsen IA, Nesbakken A, Seruca R, Gladhaug IP, Thiis-Evensen E, Rognum TO, Boberg KM, Lind GE: The novel colorectal cancer biomarkers CDO1, ZSCAN18 and ZNF331 are frequently methylated across gastrointestinal cancers. Int J Cancer 2015, 136:844–853.

The last paragraph of the Background should have read as follows:

“Zinc finger protein 331 (ZNF331) was first identified from thyroid tumors [12]. It is also known as RITA (rearranged in thyroid adenoma), ZNF361, and ZNF463 [13]. The ZNF331 gene is located at chromosome 19q13.42, a region in which loss of heterozygosity (LOH) was detected in prostate cancer [14]. In our previous study, we found that the ZNF331 gene is frequently methylated in human esophageal squamous cell cancer (ESCC) and it serves as a tumor suppressor in ESCC [15]. It was reported that the high methylation frequency of ZNF331 was found in some types of gastrointestinal cancer including CRC [16]. But the function of ZNF331 in human CRC remains unclear. In this study, we analyzed the epigenetic regulation and the function of ZNF331 in human CRC.”

Reference

  1. Wang, et al. Methylation of ZNF331 is an independent prognostic marker of colorectal cancer and promotes colorectal cancer growth. Clin Epigenetics. 2017;9:115. https://doi.org/10.1186/s13148-017-0417-4.

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Correspondence to Mingzhou Guo.

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The original article can be found online at https://doi.org/10.1186/s13148-017-0417-4.

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Wang, Y., He, T., Herman, J.G. et al. Correction to: Methylation of ZNF331 is an independent prognostic marker of colorectal cancer and promotes colorectal cancer growth. Clin Epigenet 10, 36 (2018). https://doi.org/10.1186/s13148-018-0467-2

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  • DOI: https://doi.org/10.1186/s13148-018-0467-2