Aberrant expression of tumor suppressors CADM1 and 4.1B in invasive lesions of primary breast cancer

Aberrant expression of tumor suppressors CADM1 and 4.1B in invasive lesions of primary breast cancer

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Yuka Takahashi Miwako Iwai Taketo Kawai Atsushi Arakawa Takeshi Ito Mika Sakurai-Yageta Akihiko Ito Akiteru Goto Mitsue Saito Fujio
  • چاپ و سال / کشور: 2011

Description

and DAL-1/4.1B are frequently inactivated by promoter methylation in non-small cell lung cancer. The proteins they encode, CADM1 and 4.1B, form a complex in human epithelial cells and are involved in cell–cell adhesion. Methods Expression of CADM1 and 4.1B proteins was examined by immunohistochemistry in 67 primary breast cancer and adjacent noncancerous tissues. CADM1 and 4.1B messenger RNA (mRNA) was detected by reversetranscription polymerase chain reaction (RT-PCR). The methylation status of the CADM1 and 4.1B promoters was determined quantitatively by bisulfite treatment followed by pyrosequencing. Results CADM1 and 4.1B protein signals were detected along the cell membrane in normal mammary epithelia. By contrast, 47 (70%) and 49 (73%) of 67 primary breast cancers showed aberrant CADM1 and 4.1B staining, respectively. Aberrant CADM1 staining was more frequently observed in pT2 and pT3 tumors and for stages II and III (P = 0.045 and P = 0.020, respectively), while aberrant 4.1B staining was more often observed in tumors with lymph node metastasis, for pT2 and pT3 tumors, and for stages II and III (P = 0.0058, P = 0.0098, and P = 0.0007, respectively). Furthermore, aberrant CADM1 and 4.1B expression was preferentially observed in invasive relative to noninvasive lesions from the same specimen (P = 0.036 and P = 0.0009, respectively). Finally, hypermethylation of CADM1 and 4.1B genes was detected in 46% and 42% of primary breast cancers, respectively. Conclusions Our findings suggest that aberrant CADM1 and 4.1B expression is involved in progression of breast cancer, especially in invasion into the stroma and metastasis.
Breast Cancer DOI 10.1007/s12282-011-0272-7 Received: 25 November 2010 / Accepted: 4 April 2011  The Japanese Breast Cancer Society 2011
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