Serum IL-6 Can Be a Sentinel Biomarker for Sarcopenia and Cancer Cachexia

Q3 Medicine Open Biomarkers Journal Pub Date : 2019-01-01 DOI:10.36648/2472-1646.5.1.58
Y. Kikuchi, T. Yoshikawa, T. Asakawa, M. Takano
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Abstract

Approximately 50%-80%of cancer patients have been reported to result in a devasting syndrome such as cancer cachexia (CC) and at least 20% patients reach the death [1]. Sarcopenia accompanying with muscle loss shows the most clinically relevant phenotypic feature of CC, such as asthenia, fatigue, impaired physiologic function, reduced tolerance to treatments, resulting in impaired quality of life and shorter survival. Such wasting syndromes as sarcopenia are shown in 20%-70% cases depending on the tumor type. Accordingly, reversion of CC and sarcopenia is of most importance and interest. In addition, high serum IL-6 has been reported to result in cancer metastases, invasion and resulting in CC [2,3]. Early detection of such sarcopenia syndromes is clinically most important. If sarcopenia can be precedently predicted, better treatment strategies will be possible. It is well-known that sarcopenia is accompanied by increased levels of inflammation factors TNF-alpha and IL-6 [4]. It has been reported that activation of the IL-6/STAT3 pathway also plays a causative role in the pathogenesis of cancer cachexia, one of the most distressing complications associated with the development of ovarian cancer [5]. Indeed, cachexia usually accompanies the development of ascites and chemoresistance in the most advanced stages of the disease [6]. The majority of advanced gynecologic cancer (GC) patients develop cachexia, which is a major contributor of morbidity and mortality in these patients. Cachexia is primarily responsible for body and muscle weight loss and correlates with tumor burden, increased proinflammatory cytokine levels, fatigue, and reduced response to chemotherapy and radio-therapy [7]. Patients presenting with advanced stage GC often show large tumor and ascites burden that, in turn, results into severe malnourishment because of decreased oral intake and compromised bowel functions. Despite its significant negative impact on quality of life, no effective treatment is currently available for GC-related cachexia. Indeed, muscle loss and low skeletal muscle attenuation are often detected in women undergoing primary debulking surgery for the treatment of GCs. Along the same line, recent evidence suggests that baseline sarcopenia represents one of the most accurate prognostic factors for survival in advanced GC and during chemotherapy treatment [8]. Clinically, we find out that elevation of serum IL-6 in patients with gynecologic cancers is varied by effect of the adjuvant chemotherapy.
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血清IL-6可作为肌肉减少症和癌症恶病质的前哨生物标志物
据报道,大约50%-80%的癌症患者会出现恶性综合征,如癌症恶病质(CC),至少20%的患者死亡[1]。肌少症伴肌肉损失是CC最具临床相关性的表型特征,如虚弱、疲劳、生理功能受损、对治疗的耐受性降低,导致生活质量下降,生存期缩短。根据肿瘤类型不同,20%-70%的病例会出现肌肉减少症等消瘦综合征。因此,CC和肌肉减少症的逆转是最重要和最感兴趣的。此外,高血清IL-6有报道可导致癌症转移、侵袭并导致CC[2,3]。早期发现这种肌肉减少综合征在临床上是最重要的。如果肌肉减少症可以预先预测,更好的治疗策略将是可能的。众所周知,肌肉减少症伴随着炎症因子tnf - α和IL-6水平的升高[4]。据报道,IL-6/STAT3通路的激活也在癌症恶病质的发病机制中起着致病作用,恶病质是卵巢癌发展中最令人痛苦的并发症之一[5]。事实上,在疾病的晚期,恶病质通常伴随着腹水和化疗耐药的发展[6]。大多数晚期妇科癌症(GC)患者出现恶病质,这是这些患者发病率和死亡率的主要因素。恶病质是机体和肌肉体重减轻的主要原因,并与肿瘤负荷、促炎细胞因子水平升高、疲劳以及对化疗和放疗反应降低相关[7]。晚期胃癌患者通常表现为大肿瘤和腹水负担,这反过来又导致严重的营养不良,因为口服摄入量减少和肠道功能受损。尽管gc相关恶病质对生活质量有显著的负面影响,但目前尚无有效的治疗方法。事实上,在接受原发性减体积手术治疗GCs的妇女中经常发现肌肉损失和低骨骼肌衰减。同样,最近的证据表明,基线肌少症是晚期胃癌患者和化疗期间最准确的预后因素之一[8]。临床上,我们发现妇科肿瘤患者血清IL-6的升高随辅助化疗的效果而变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Open Biomarkers Journal
Open Biomarkers Journal Medicine-Medicine (miscellaneous)
CiteScore
0.80
自引率
0.00%
发文量
9
期刊介绍: The Open Biomarkers Journal is an Open Access online journal, which publishes original full-length, short research articles and reviews on biomarkers in clinical, medical and pharmaceutical research. The coverage includes biomarkers of disease, new biomarkers, exposure to drugs, genetic effects, and applications of biomarkers. The Open Biomarkers Journal, a peer reviewed journal, aims to provide the most complete and reliable source of information on current developments in the field. The emphasis will be on publishing quality articles rapidly and freely available to researchers worldwide.
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