BibTex RIS Kaynak Göster

Molecular basis of the triple negative breast cancer

Yıl 2015, Cilt: 24 Sayı: 2, 251 - 259, 05.03.2015
https://doi.org/10.17827/aktd.80326

Öz

Breast cancer is the most common type of cancer in women and more than 1 million breast cancer cases are diagnosed each year all over the world. Breast cancer is a complex and heterogeneous disease in terms of its molecular structure, mutation type, metastase properties, clinical course and therapeutic response. Breast cancer is divided into subtypes based on expression properties of molecular markers as estrogen receptor, progestron receptor, human epidermal growth factor receptor 2. Triple-negative breast cancer is characterized by the lack of tumors that estrogen receptor, progestron receptor, human epidermal growth factor receptor 2 gene expression. These type of tumors lead to agressive clinical course due to unresponsiveness to systemic endocrine therapy and poor prognosis. Triple negative breast cancer constitutes 10-20% of all breast cancers. It affects generally young and African-American women. Triple negative breast cancer have several subtypes based on the gene expression properties. The majority of them are basal-like breast cancers. In this review, current literature is revised and summarized with respect to the molecular basis of triple negative cancers.

Kaynakça

  • Ismail-Khan R, Bui MM. A review of triple-negative breast cancer. Cancer Control. 2010;17:173-6.
  • de Ruijter TC, Veeck J, de Hoon JP, van Engeland M, Tjan-Heijnen VC. Characteristics of triple- negative breast cancer. J Cancer Res Clin Oncol. 2011;137:183-92.
  • Reddy KB.Triple-negative breast cancers: an updated review on treatment options. Curr Oncol. 2011;18:73-9.
  • Gluz O, Liedtke C, Gottschalk N, Pusztai L, Nitz U, Harbeck N. Triple-negative breast cancer-- current status and future directions. Ann Oncol. 2009;20:1913-27.
  • Stevens KN, Vachon CM, Couch FJ. Genetic susceptibility to triple-negative breast cancer. Cancer Res. 2013;73:2025-30.
  • Lehmann BD, Bauer JA, Chen X, Sanders ME, Chakravarthy AB, Shyr Y et al. Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies.J Clin Invest. 2011;121:2750-67.
  • Penault-Llorca F, Viale G. Pathological and molecular diagnosis of triple-negative breast cancer: a clinical perspective. Ann Oncol. 2012;23:19-22.
  • Peng Y. Potential prognostic tumor biomarkers in triple-negative breast carcinoma. Beijing Da Xue Xue Bao. 2012; 18:666-72.
  • Engebraaten O, Vollan HK, Bİrresen-Dale AL. Triple-negative breast cancer and the need for new therapeutic targets. Am J Pathol. 2013;183:1064-74.
  • Peddi PF, Ellis MJ, Ma C. Molecular basis of triple negative breast cancer and implications for therapy. Int J Breast Cancer. 2012;217185.
  • Criscitiello C, Azim HA Jr, Schouten PC, Linn SC, Sotiriou C. Understanding the biology of triple- negative breast cancer. Ann Oncol. 2012;23:13-8.
  • Brady-West DC, McGrowder DA. Triple negative breast cancer: therapeutic and prognostic implications. Asian Pac J Cancer Prev. 2011;12:2139-43.
  • Carey LA. Directed therapy of subtypes of triple-negative breast cancer. Oncologist. 2010;15:49- 56.
  • Prat A, Adamo B, Cheang MC, Anders CK, Carey LA, Perou CM. Molecular characterization of basal- like and non-basal-like triple-negative breast cancer. Oncologist. 2013;18:123-33.
  • Elsawaf Z, Sinn HP. Triple-negative breast cancer: clinical and histological correlations. Breast Care (Basel). 2011;6:273-8.
  • Kuo WH, Chang YY, Lai LC, Tsai MH, Hsiao CK, Chang KJ et al. Molecular characteristics and metastasis predictor genes of triple-negative breast cancer: a clinical study of triple-negative breast carcinomas. PLoS One. 2012;7:e45831.
  • Lu S, Singh K, Mangray S, Tavares R, Noble L, Resnick MB et al. Claudin expression in high-grade invasive ductal carcinoma of the breast: correlation with the molecular subtype. Mod Pathol. 2013;26:485-95.
  • Anders CK, Zagar TM, Carey LA. The management of early-stage and metastatic triple-negative breast cancer: a review.Hematol Oncol Clin North Am. 2013;27:737-49.
  • Hosford SR, Miller TW. Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways .Pharmgenomics Pers Med. 2014;7:203- 15.
  • Yuan ZY, Dai T, Wang SS, Peng RJ, Li XH, Qin T et al. Overexpression of ETV4 protein in triple- negative breast cancer is associated with a higher risk of distant metastasis. Onco Targets Ther. 2014;7:1733-42.
  • Eichelser C, Stückrath I, Müller V, Milde-Langosch K, Wikman H, Pantel K et al. Increased serum levels of circulating exosomal microRNA-373 in receptor-negative breast cancer patients. Oncotarget. 2014;5:9650-63.
  • D'Ippolito E, Iorio MV. MicroRNAs and triple negative breast cancer. Int J Mol Sci. 2013;14:22202- 20.
  • Radojicic J, Zaravinos A, Vrekoussis T, Kafousi M, Spandidos DA, Stathopoulos EN. MicroRNA expression analysis in triple-negative (ER, PR and Her2/neu) breast cancer. Cell Cycle. 2011;10:507-17.
  • Phipps AI, Li CI. Breastfeeding and triple-negative breast cancer: potential implications for racial/ethnic disparities. J Natl Cancer Inst. 2014;15:106(10):pii, dju281.
  • Fernandez SV, Bingham C, Fittipaldi P, Austin L, Palazzo J, Palmer G et al. TP53 mutations detected in circulating tumor cells present in the blood of metastatic triple negative breast cancer patients. Breast Cancer Res. 2014;16:445.
  • Davis SL, Eckhardt SG, Tentler JJ, Diamond JR. Triple-negative breast cancer: bridging the gap from cancer genomics to predictive biomarkers. Ther Adv Med Oncol. 2014;6:88-100.
  • Hosford SR, Miller TW. Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways. Pharmgenomics Pers Med. 2014;7:203-15.
  • Correspondence Address / Yazışma Adresi

Triple Negatif Meme Kanserinin Moleküler Temeli

Yıl 2015, Cilt: 24 Sayı: 2, 251 - 259, 05.03.2015
https://doi.org/10.17827/aktd.80326

Öz

Meme kanseri kadınlarda en çok görülen kanser türüdür ve her yıl tüm dünyada 1 milyondan fazla meme kanseri tanısı konmaktadır. Moleküler yapı, mutasyon tipi, metastaz özelliği, klinik gidiş ve tedaviye cevap açısından karışık ve heterojen bir hastalıktır. Meme kanseri estrogen receptor (ER) / progestron reseptor (PR) / Human epidermal growth factor receptor 2 (HER-2) proteinlerine ait moleküler belirteçlerinin ekspresyon özelliğine göre alt tiplere ayrılmaktadır. Triple negatif meme kanseri (TNMK) tümörün ER / PR / HER2 ekspresyonu olmayışı ile karekterizedir. Bu tip tümörler sistemik endokrin tedaviye yanıt vermeyişi ve kötü prognoz nedeniyle agresif klinik seyir gösterir. TNMK tüm meme kanserlerinin %15-20’ni oluşturur, sıklıkla genç yaştakileri ve Afrikalı kadınları etkiler. TNMK ekspresyon özelliğine göre alt tiplere ayrılır ve çoğunluğunu Bazal-like meme kanserleri (BLMK) oluşturur. Bu derlemede, TNMK’nın moleküler temeli hakkındaki son literatür gözden geçirilecektir

Kaynakça

  • Ismail-Khan R, Bui MM. A review of triple-negative breast cancer. Cancer Control. 2010;17:173-6.
  • de Ruijter TC, Veeck J, de Hoon JP, van Engeland M, Tjan-Heijnen VC. Characteristics of triple- negative breast cancer. J Cancer Res Clin Oncol. 2011;137:183-92.
  • Reddy KB.Triple-negative breast cancers: an updated review on treatment options. Curr Oncol. 2011;18:73-9.
  • Gluz O, Liedtke C, Gottschalk N, Pusztai L, Nitz U, Harbeck N. Triple-negative breast cancer-- current status and future directions. Ann Oncol. 2009;20:1913-27.
  • Stevens KN, Vachon CM, Couch FJ. Genetic susceptibility to triple-negative breast cancer. Cancer Res. 2013;73:2025-30.
  • Lehmann BD, Bauer JA, Chen X, Sanders ME, Chakravarthy AB, Shyr Y et al. Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies.J Clin Invest. 2011;121:2750-67.
  • Penault-Llorca F, Viale G. Pathological and molecular diagnosis of triple-negative breast cancer: a clinical perspective. Ann Oncol. 2012;23:19-22.
  • Peng Y. Potential prognostic tumor biomarkers in triple-negative breast carcinoma. Beijing Da Xue Xue Bao. 2012; 18:666-72.
  • Engebraaten O, Vollan HK, Bİrresen-Dale AL. Triple-negative breast cancer and the need for new therapeutic targets. Am J Pathol. 2013;183:1064-74.
  • Peddi PF, Ellis MJ, Ma C. Molecular basis of triple negative breast cancer and implications for therapy. Int J Breast Cancer. 2012;217185.
  • Criscitiello C, Azim HA Jr, Schouten PC, Linn SC, Sotiriou C. Understanding the biology of triple- negative breast cancer. Ann Oncol. 2012;23:13-8.
  • Brady-West DC, McGrowder DA. Triple negative breast cancer: therapeutic and prognostic implications. Asian Pac J Cancer Prev. 2011;12:2139-43.
  • Carey LA. Directed therapy of subtypes of triple-negative breast cancer. Oncologist. 2010;15:49- 56.
  • Prat A, Adamo B, Cheang MC, Anders CK, Carey LA, Perou CM. Molecular characterization of basal- like and non-basal-like triple-negative breast cancer. Oncologist. 2013;18:123-33.
  • Elsawaf Z, Sinn HP. Triple-negative breast cancer: clinical and histological correlations. Breast Care (Basel). 2011;6:273-8.
  • Kuo WH, Chang YY, Lai LC, Tsai MH, Hsiao CK, Chang KJ et al. Molecular characteristics and metastasis predictor genes of triple-negative breast cancer: a clinical study of triple-negative breast carcinomas. PLoS One. 2012;7:e45831.
  • Lu S, Singh K, Mangray S, Tavares R, Noble L, Resnick MB et al. Claudin expression in high-grade invasive ductal carcinoma of the breast: correlation with the molecular subtype. Mod Pathol. 2013;26:485-95.
  • Anders CK, Zagar TM, Carey LA. The management of early-stage and metastatic triple-negative breast cancer: a review.Hematol Oncol Clin North Am. 2013;27:737-49.
  • Hosford SR, Miller TW. Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways .Pharmgenomics Pers Med. 2014;7:203- 15.
  • Yuan ZY, Dai T, Wang SS, Peng RJ, Li XH, Qin T et al. Overexpression of ETV4 protein in triple- negative breast cancer is associated with a higher risk of distant metastasis. Onco Targets Ther. 2014;7:1733-42.
  • Eichelser C, Stückrath I, Müller V, Milde-Langosch K, Wikman H, Pantel K et al. Increased serum levels of circulating exosomal microRNA-373 in receptor-negative breast cancer patients. Oncotarget. 2014;5:9650-63.
  • D'Ippolito E, Iorio MV. MicroRNAs and triple negative breast cancer. Int J Mol Sci. 2013;14:22202- 20.
  • Radojicic J, Zaravinos A, Vrekoussis T, Kafousi M, Spandidos DA, Stathopoulos EN. MicroRNA expression analysis in triple-negative (ER, PR and Her2/neu) breast cancer. Cell Cycle. 2011;10:507-17.
  • Phipps AI, Li CI. Breastfeeding and triple-negative breast cancer: potential implications for racial/ethnic disparities. J Natl Cancer Inst. 2014;15:106(10):pii, dju281.
  • Fernandez SV, Bingham C, Fittipaldi P, Austin L, Palazzo J, Palmer G et al. TP53 mutations detected in circulating tumor cells present in the blood of metastatic triple negative breast cancer patients. Breast Cancer Res. 2014;16:445.
  • Davis SL, Eckhardt SG, Tentler JJ, Diamond JR. Triple-negative breast cancer: bridging the gap from cancer genomics to predictive biomarkers. Ther Adv Med Oncol. 2014;6:88-100.
  • Hosford SR, Miller TW. Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways. Pharmgenomics Pers Med. 2014;7:203-15.
  • Correspondence Address / Yazışma Adresi
Toplam 28 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Derleme
Yazarlar

Ayşe Feyda Nursal

Yayımlanma Tarihi 5 Mart 2015
Yayımlandığı Sayı Yıl 2015 Cilt: 24 Sayı: 2

Kaynak Göster

AMA Nursal AF. Molecular basis of the triple negative breast cancer. aktd. Haziran 2015;24(2):251-259. doi:10.17827/aktd.80326