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. 2017 Feb 1;18(2):310. doi: 10.3390/ijms18020310

Table 1.

Aberrant gene expressions and related molecular mechanisms in parathyroid carcinomas compared with normal parathyroid glands.

Gene ID Chr. Map Gene Function Variation in PCas Frequency in PCas
Loss of function mutated genes
CDC73 1q31.2 Tumor suppressor involved in transcriptional and post-transcriptional control 70%
PRUNE2 9q21.2 Tumor suppressor involved in the suppression of Ras homolog family member A activity 18%
MEN1 11q12 Tumor suppressor associated with MEN1 syndrome 13%
Hypermethylated genes
HIC1 17p13 Tumor suppressor involved in inhibition of E2F1 through interaction with SIRT1 100%
APC 5q22.2 Tumor suppressor, inhibitor of the Wnt/β-catenin pathway 33%–100%
RASSF1A 3p21.31 Ras-association domain family 1 100%
SFRP1 8p11.21 Secreted frizzled related protein 1, inhibitor of the Wnt/β-catenin pathway 100%
SFRP2 4q31.3 Secreted frizzled related protein 2, inhibitor of the Wnt/β-catenin pathway n.a.
SFRP4 7p14.1 Secreted frizzled related protein 4, inhibitor of the Wnt/β-catenin pathway n.a.
CDKN2A/p16 9p21.3 Cyclin-dependent kinase inhibitor n.a.
CDKN2B/p15 9p21.3 Cyclin-dependent kinase inhibitor n.a.
WT1 11p13 Wilms tumor 1, tumor suppressor n.a.
Hypomethylated genes
C19MC 19q13.42 microRNA cluster 58%
Aberrantly expressed chromatin remodeling genes
HIST1H1C 6p22.2 Replication-dependent histone H1.2 100%
HIST1H2AB 6p22.2 Replication-dependent histone H2A n.a.
HIST1H2BB 6p22.2 Replication-dependent histone H2B n.a.
EZH2 7q36.1 Enhancer of zeste 2 polycomb repressive complex 2 subunit 100%

Chr., chromosome; PCas, parathyroid carcinomas; CDC73, cell division cycle 73; APC, Wnt signaling pathway regulator; PRUNE2, prune homolog 2; MEN1, multiple endocrine neoplasia type 1 syndrome; HIC1, hypermethylated in human cancers 1; SIRT1, sirtuin 1; C19MC, chromosome 19 microRNA cluster; n.a., not available.