Biomarkers in cancer最新文献

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Deep Sequencing of Serum Small RNAs Identifies Patterns of 5' tRNA Half and YRNA Fragment Expression Associated with Breast Cancer. 血清小rna深度测序鉴定与乳腺癌相关的5' tRNA半和YRNA片段表达模式
Biomarkers in cancer Pub Date : 2014-12-08 eCollection Date: 2014-01-01 DOI: 10.4137/BIC.S20764
Joseph M Dhahbi, Stephen R Spindler, Hani Atamna, Dario Boffelli, David Ik Martin
{"title":"Deep Sequencing of Serum Small RNAs Identifies Patterns of 5' tRNA Half and YRNA Fragment Expression Associated with Breast Cancer.","authors":"Joseph M Dhahbi,&nbsp;Stephen R Spindler,&nbsp;Hani Atamna,&nbsp;Dario Boffelli,&nbsp;David Ik Martin","doi":"10.4137/BIC.S20764","DOIUrl":"https://doi.org/10.4137/BIC.S20764","url":null,"abstract":"<p><p>Small noncoding RNAs circulating in the blood may serve as signaling molecules because of their ability to carry out a variety of cellular functions. We have previously described tRNA- and YRNA-derived small RNAs circulating as components of larger complexes in the blood of humans and mice; the characteristics of these small RNAs imply specific processing, secretion, and physiological regulation. In this study, we have asked if changes in the serum abundance of these tRNA and YRNA fragments are associated with a diagnosis of cancer. We used deep sequencing and informatics analysis to catalog small RNAs in the sera of breast cancer cases and normal controls. 5' tRNA halves and YRNA fragments are abundant in both groups, but we found that a breast cancer diagnosis is associated with changes in levels of specific subtypes. This prompted us to look at existing sequence datasets of serum small RNAs from 42 breast cancer cases, taken at the time of diagnosis. We find significant changes in the levels of specific 5' tRNA halves and YRNA fragments associated with clinicopathologic characteristics of the cancer. Although these findings do not establish causality, they suggest that circulating 5' tRNA halves and YRNA fragments with known cellular functions may participate in breast cancer syndromes and have potential as circulating biomarkers. Larger studies with multiple types of cancer are needed to adequately evaluate their potential use for the development of noninvasive cancer screening. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"6 ","pages":"37-47"},"PeriodicalIF":0.0,"publicationDate":"2014-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S20764","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32918921","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 145
Allele and genotype distributions of DNA repair gene polymorphisms in South Indian healthy population. 南印度健康人群DNA修复基因多态性的等位基因和基因型分布。
Biomarkers in cancer Pub Date : 2014-12-07 eCollection Date: 2014-01-01 DOI: 10.4137/BIC.S19681
Katiboina Srinivasa Rao, Abialbon Paul, Annan Sudarsan Arun Kumar, Gurusamy Umamaheswaran, Biswajit Dubashi, Karunanithi Gunaseelan, Steven Aibor Dkhar
{"title":"Allele and genotype distributions of DNA repair gene polymorphisms in South Indian healthy population.","authors":"Katiboina Srinivasa Rao,&nbsp;Abialbon Paul,&nbsp;Annan Sudarsan Arun Kumar,&nbsp;Gurusamy Umamaheswaran,&nbsp;Biswajit Dubashi,&nbsp;Karunanithi Gunaseelan,&nbsp;Steven Aibor Dkhar","doi":"10.4137/BIC.S19681","DOIUrl":"https://doi.org/10.4137/BIC.S19681","url":null,"abstract":"<p><p>Various DNA repair pathways protect the structural and chemical integrity of the human genome from environmental and endogenous threats. Polymorphisms of genes encoding the proteins involved in DNA repair have been found to be associated with cancer risk and chemotherapeutic response. In this study, we aim to establish the normative frequencies of DNA repair genes in South Indian healthy population and compare with HapMap populations. Genotyping was done on 128 healthy volunteers from South India, and the allele and genotype distributions were established. The minor allele frequency of Xeroderma pigmentosum group A (XPA) G23A, Excision repair cross-complementing 2 (ERCC2)/Xeroderma pigmentosum group D (XPD) Lys751Gln, Xeroderma pigmentosum group G (XPG) His46His, XPG Asp1104His, and X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln polymorphisms were 49.2%, 36.3%, 48.0%, 23.0%, and 34.0% respectively. Ethnic variations were observed in the frequency distribution of these polymorphisms between the South Indians and other HapMap populations. The present work forms the groundwork for cancer association studies and biomarker identification for treatment response and prognosis. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"6 ","pages":"29-35"},"PeriodicalIF":0.0,"publicationDate":"2014-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S19681","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32918920","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
A standardized and reproducible urine preparation protocol for cancer biomarkers discovery. 一个标准化和可重复的尿液制备方案,用于癌症生物标志物的发现。
Biomarkers in cancer Pub Date : 2014-11-03 eCollection Date: 2014-01-01 DOI: 10.4137/BIC.S17991
Julia Beretov, Valerie C Wasinger, Peter Schwartz, Peter H Graham, Yong Li
{"title":"A standardized and reproducible urine preparation protocol for cancer biomarkers discovery.","authors":"Julia Beretov,&nbsp;Valerie C Wasinger,&nbsp;Peter Schwartz,&nbsp;Peter H Graham,&nbsp;Yong Li","doi":"10.4137/BIC.S17991","DOIUrl":"https://doi.org/10.4137/BIC.S17991","url":null,"abstract":"<p><p>A suitable and standardized protein purification technique is essential to maintain consistency and to allow data comparison between proteomic studies for urine biomarker discovery. Ultimately, efforts should be made to standardize urine preparation protocols. The aim of this study was to develop an optimal analytical protocol to achieve maximal protein yield and to ensure that this method was applicable to examine urine protein patterns that distinguish disease and disease-free states. In this pilot study, we compared seven different urine sample preparation methods to remove salts, and to precipitate and isolate urinary proteins. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) profiles showed that the sequential preparation of urinary proteins by combining acetone and trichloroacetic acid (TCA) alongside high speed centrifugation (HSC) provided the best separation, and retained the most urinary proteins. Therefore, this approach is the preferred method for all further urine protein analysis. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"6 ","pages":"21-7"},"PeriodicalIF":0.0,"publicationDate":"2014-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S17991","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32862413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
Biomarkers of HIV-associated Cancer. hiv相关癌症的生物标志物。
Biomarkers in cancer Pub Date : 2014-07-03 eCollection Date: 2014-01-01 DOI: 10.4137/BIC.S15056
Brian Thabile Flepisi, Patrick Bouic, Gerhard Sissolak, Bernd Rosenkranz
{"title":"Biomarkers of HIV-associated Cancer.","authors":"Brian Thabile Flepisi,&nbsp;Patrick Bouic,&nbsp;Gerhard Sissolak,&nbsp;Bernd Rosenkranz","doi":"10.4137/BIC.S15056","DOIUrl":"https://doi.org/10.4137/BIC.S15056","url":null,"abstract":"<p><p>Cancer biomarkers have provided great opportunities for improving the management of cancer patients by enhancing the efficiency of early detection, diagnosis, and efficacy of treatment. Every cell type has a unique molecular signature, referred to as biomarkers, which are identifiable characteristics such as levels or activities of a myriad of genes, proteins, or other molecular features. Biomarkers can facilitate the molecular definition of cancer, provide information about the course of cancer, and predict response to chemotherapy. They offer the hope of early detection as well as tracking disease progression and recurrence. Current progress in the characterization of molecular genetics of HIV-associated cancers may form the basis for improved patient stratification and future targeted or individualized therapies. Biomarker use for cancer staging and personalization of therapy at the time of diagnosis could improve patient care. This review focuses on the relevance of biomarkers in the most common HIV-associated malignancies, namely, Kaposi sarcoma, non-Hodgkin's lymphoma, and invasive cervical cancer. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"6 ","pages":"11-20"},"PeriodicalIF":0.0,"publicationDate":"2014-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S15056","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32530418","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
Differential expression of cysteine dioxygenase 1 in complex karyotype liposarcomas. 半胱氨酸双加氧酶1在复杂核型脂肪肉瘤中的差异表达。
Biomarkers in cancer Pub Date : 2014-04-06 eCollection Date: 2014-01-01 DOI: 10.4137/BIC.S14683
Mohammed Shaker, Kara M Pascarelli, Matthew J Plantinga, Miles A Love, Alexander J Lazar, Davis R Ingram, Margaret von Mehren, Dina Lev, David Kipling, Dominique Broccoli
{"title":"Differential expression of cysteine dioxygenase 1 in complex karyotype liposarcomas.","authors":"Mohammed Shaker,&nbsp;Kara M Pascarelli,&nbsp;Matthew J Plantinga,&nbsp;Miles A Love,&nbsp;Alexander J Lazar,&nbsp;Davis R Ingram,&nbsp;Margaret von Mehren,&nbsp;Dina Lev,&nbsp;David Kipling,&nbsp;Dominique Broccoli","doi":"10.4137/BIC.S14683","DOIUrl":"https://doi.org/10.4137/BIC.S14683","url":null,"abstract":"<p><p>Altered cysteine dioxygenase 1 (CDO1) gene expression has been observed in several cancers but has not yet been investigated in liposarcomas. The aim of this study was to evaluate CDO1 expression in a cohort of liposarcomas and to determine its association with clinicopathological features. Existing microarray data indicated variable CDO1 expression in liposarcoma subtypes. CDO1 mRNA from a larger cohort of liposarcomas was quantified by real time-PCR, and CDO1 protein expression was determined by immunohistochemistry (IHC) in more than 300 tumor specimens. Well-differentiated liposarcomas (WDLSs) had significantly higher CDO1 gene expression and protein levels than dedifferentiated liposarcomas (DDLSs) (P < 0.001). Location of the tumor was not predictive of the expression level of CDO1 mRNA in any histological subtype of liposarcoma. Recurrent tumors did not show any difference in CDO1 expression when compared to primary tumors. CDO1 expression was upregulated as human mesenchymal stem cells (hMSCs) undergo differentiation into mature adipocytes. Our results suggest that CDO1 is a marker of liposarcoma progression and adipogenic differentiation. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"6 ","pages":"1-10"},"PeriodicalIF":0.0,"publicationDate":"2014-04-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S14683","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32271056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
An Antibody-based Blood Test Utilizing a Panel of Biomarkers as a New Method for Improved Breast Cancer Diagnosis. 利用一组生物标志物作为改进乳腺癌诊断的新方法的基于抗体的血液检测。
Biomarkers in cancer Pub Date : 2013-11-19 eCollection Date: 2013-01-01 DOI: 10.4137/BIC.S13236
Galit Yahalom, Daria Weiss, Ilya Novikov, Therese B Bevers, Laszlo G Radvanyi, Mei Liu, Benjamin Piura, Stefano Iacobelli, Maria T Sandri, Enrico Cassano, Tanir M Allweis, Arie Bitterman, Pnina Engelman, Luis M Vence, Marvin M Rosenberg
{"title":"An Antibody-based Blood Test Utilizing a Panel of Biomarkers as a New Method for Improved Breast Cancer Diagnosis.","authors":"Galit Yahalom,&nbsp;Daria Weiss,&nbsp;Ilya Novikov,&nbsp;Therese B Bevers,&nbsp;Laszlo G Radvanyi,&nbsp;Mei Liu,&nbsp;Benjamin Piura,&nbsp;Stefano Iacobelli,&nbsp;Maria T Sandri,&nbsp;Enrico Cassano,&nbsp;Tanir M Allweis,&nbsp;Arie Bitterman,&nbsp;Pnina Engelman,&nbsp;Luis M Vence,&nbsp;Marvin M Rosenberg","doi":"10.4137/BIC.S13236","DOIUrl":"https://doi.org/10.4137/BIC.S13236","url":null,"abstract":"<p><p>In order to develop a new tool for diagnosis of breast cancer based on autoantibodies against a panel of biomarkers, a clinical trial including blood samples from 507 subjects was conducted. All subjects showed a breast abnormality on exam or breast imaging and final biopsy pathology of either breast cancer patients or healthy controls. Using an enzyme-linked immunosorbent assay, the samples were tested for autoantibodies against a predetermined number of biomarkers in various models that were used to determine a diagnosis, which was compared to the clinical status. Our new assay achieved a sensitivity of 95.2% [CI = 92.8-96.8%] at a fixed specificity of 49.5%. Receiver-operator characteristic curve analysis showed an area under the curve of 80.1% [CI = 72.6-87.6%]. These results suggest that a blood test which is based on models comprising several autoantibodies to specific biomarkers may be a new and novel tool for improving the diagnostic evaluation of breast cancer. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"5 ","pages":"71-80"},"PeriodicalIF":0.0,"publicationDate":"2013-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S13236","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31943643","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
Molecular profiling for breast cancer: a comprehensive review. 乳腺癌的分子分析:一个全面的综述。
Biomarkers in cancer Pub Date : 2013-10-29 DOI: 10.4137/BIC.S9455
Muaiad Kittaneh, Alberto J Montero, Stefan Glück
{"title":"Molecular profiling for breast cancer: a comprehensive review.","authors":"Muaiad Kittaneh,&nbsp;Alberto J Montero,&nbsp;Stefan Glück","doi":"10.4137/BIC.S9455","DOIUrl":"https://doi.org/10.4137/BIC.S9455","url":null,"abstract":"<p><p>In recent years advances in molecular biology have launched disruptive innovations in breast cancer diagnostics and therapeutics. The advent of genomics has revolutionized our understanding of breast cancer as several different biologically and molecularly distinct diseases. This research has led to commercially available polymerase chain reaction (PCR) and microarray tests that have begun to fundamentally change the way medical oncologists quantify recurrence risk in early stage breast cancer patients. The Genomics era has altered the clinicopathologic paradigm of selecting patients for adjuvant cytotoxic chemotherapy. Sufficiently powered prospective studies are underway that may establish these molecular assays as elements of standard clinical practice in breast cancer treatment. In this article, we review the strengths and limitations of currently available breast cancer-specific molecular tests. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"5 ","pages":"61-70"},"PeriodicalIF":0.0,"publicationDate":"2013-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S9455","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31880590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 161
Can immunohistochemistry serve as an alternative to subjective histopathological diagnosis of oral epithelial dysplasia? 免疫组织化学可以替代口腔上皮发育不良的主观组织病理学诊断吗?
Biomarkers in cancer Pub Date : 2013-10-10 DOI: 10.4137/BIC.S12951
Ahmad A Abdulmajeed, Camile S Farah
{"title":"Can immunohistochemistry serve as an alternative to subjective histopathological diagnosis of oral epithelial dysplasia?","authors":"Ahmad A Abdulmajeed,&nbsp;Camile S Farah","doi":"10.4137/BIC.S12951","DOIUrl":"https://doi.org/10.4137/BIC.S12951","url":null,"abstract":"<p><p>Many attempts have been made to identify objective molecular biomarkers to diagnose and prognosticate oral epithelial dysplasia (OED) because histopathological interpretation is subjective and lacks sensitivity. The majority of these efforts describe changes in gene expression at protein level in OED as determined by immunohistochemistry (IHC). However, the literature on these putative markers of oral cancer progression is vast and varied. The main purpose of this article is to review current knowledge on biomarkers of protein expression for OED by IHC approaches. We further discuss these findings in terms of the proposed essential hallmarks of cancer cells to better understand their role in oral oncogenesis. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"5 ","pages":"49-60"},"PeriodicalIF":0.0,"publicationDate":"2013-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S12951","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31824210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 23
Susceptibility to Cutaneous Squamous Cell Carcinoma in Renal Transplant Recipients Associates with Genes Regulating Melanogenesis Independent of their Role in Pigmentation. 肾移植受者对皮肤鳞状细胞癌的易感性与调节黑色素形成的基因相关,而与色素沉着无关。
Biomarkers in cancer Pub Date : 2013-10-07 eCollection Date: 2013-01-01 DOI: 10.4137/BIC.S12754
Per A Andresen, Dag A Nymoen, Kristina Kjærheim, Torbjørn Leivestad, Per Helsing
{"title":"Susceptibility to Cutaneous Squamous Cell Carcinoma in Renal Transplant Recipients Associates with Genes Regulating Melanogenesis Independent of their Role in Pigmentation.","authors":"Per A Andresen,&nbsp;Dag A Nymoen,&nbsp;Kristina Kjærheim,&nbsp;Torbjørn Leivestad,&nbsp;Per Helsing","doi":"10.4137/BIC.S12754","DOIUrl":"https://doi.org/10.4137/BIC.S12754","url":null,"abstract":"<p><p>The highly polymorphic melanocortin 1 receptor (MC1R) gene plays a crucial role in pigmentation. Variants of the gene have been implicated in risk of cutaneous squamous cell carcinoma (SCC) in the general population. In renal transplant (RT) recipients these cancers are more aggressive and very common. To evaluate the risk of SCC relative to MC1R and the pigmentation-associated genes ASIP, TYR, and TYRP1, a group of 217 RT recipients with and without SCC was genotyped. Associations with SCC risk were indicated in carriers of the red hair color associated MC1R variant p.Arg151Cys (OR = 1.99; 1.05-3.75), and in carriers of two of any of the MC1R variants disclosed (OR = 2.36; 1.08-5.15). These associations appeared independent of traditionally protective phenotypes, also supported by the stratifications from skin phototype and hair color. A tendency towards an increased SCC risk was observed for a specific ASIP haplotype (OR = 1.87; 0.91-3.83), while no such associations were observed for the TYR and TYRP1 variants. Thus, the risk of developing SCC in RT patients is modulated by MC1R variation irrespective of phenotypes considered to be protective. Heterozygous combinations of MC1R variants appear to be more relevant in assessing SCC risk than the effects of variants individually. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"5 ","pages":"41-7"},"PeriodicalIF":0.0,"publicationDate":"2013-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S12754","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31824208","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Circulating HER2 Extracellular Domain: A Specific and Quantitative Biomarker of Prognostic Value in all Breast Cancer Patients? 循环HER2细胞外结构域:所有乳腺癌患者预后价值的特异性定量生物标志物?
Biomarkers in cancer Pub Date : 2013-08-12 DOI: 10.4137/BIC.S12389
Walter P Carney, Dirk Bernhardt, Bharat Jasani
{"title":"Circulating HER2 Extracellular Domain: A Specific and Quantitative Biomarker of Prognostic Value in all Breast Cancer Patients?","authors":"Walter P Carney,&nbsp;Dirk Bernhardt,&nbsp;Bharat Jasani","doi":"10.4137/BIC.S12389","DOIUrl":"https://doi.org/10.4137/BIC.S12389","url":null,"abstract":"<p><p>The HER2 oncoprotein has emerged as an essential biomarker in the treatment of breast cancer patients. Once the primary breast cancer is removed, there is an increasing need to detect breast cancer recurrence as early as possible with the hope that earlier intervention with new anti-HER2 therapies will improve quality of life and increase overall survival. Numerous publications have shown that increasing blood levels of circulating HER2 is an early indicator of progression, particularly in HER2-positive patients and that the rise and fall parallels the clinical course of disease and independent of therapy. Many studies show that the HER2 status of the primary tumor may not fully and accurately reflect the HER2 status of recurrent cancer. Thus, elevated serum HER2 levels may be an early signal of the emergence of a HER2-positive metastatic tumor and therefore alert the physician to re-assess HER2 status using a tissue test. </p>","PeriodicalId":72377,"journal":{"name":"Biomarkers in cancer","volume":"5 ","pages":"31-9"},"PeriodicalIF":0.0,"publicationDate":"2013-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/BIC.S12389","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31824257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 40
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