Tambaro Federica, Imbimbo Giovanni, Pace Valentina, Amabile Maria Ida, Rizzo Veronica, Orlando Simona, Lauteri Giulia, Ramaccini Cesarina, Catalano Carlo, Nigri Giuseppe, Muscaritoli Maurizio, Molfino Alessio
Deparment of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Department of Surgery, Sapienza University of Rome, Rome, Italy.
Front Mol Biosci. 2024 Jul 30;11:1449197. doi: 10.3389/fmolb.2024.1449197. eCollection 2024.
Adipose tissue (AT) wasting in cancer is an early catabolic event with negative impact on outcomes. Circulating miRNAs may promote body weight loss and cachexia. We measured circulating miRNAs linked to AT alterations and compared their levels between i) gastrointestinal (GI) cancer patients and controls, ii) cachectic and non-cachectic cancer patients, and iii) according to adiposity level and its distribution.
Patients with GI cancer and subjects with benign diseases as controls were considered. Cachexia was assessed and adiposity evaluated by CT-scan for subcutaneous AT area (SAT), visceral AT area and the total AT area (TAT). MiRNAs involved were measured in plasma by RT-qPCR.
37 naïve GI cancer patients and 14 controls were enrolled. Patients with cachexia presented with lower SAT compared to non-cachectic ( < 0.05). In cancer patients, we found higher levels of miR-26a, miR-128, miR-155 and miR-181a vs. controls ( < 0.05). Cancer patients with BMI 25 kg/m showed higher levels of miR-26a vs. those with BMI 25 ( = 0.035). MiR-26a and miR-181a were higher in cachectic and non-cachectic vs. controls ( < 0.05). Differences between cachectic and controls were confirmed for miR-155 ( < 0.001) but not between non-cachectic vs. control ( = 0.072). MiR-155 was higher in cachectic patients with low TAT vs. those without cachexia and high TAT ( = 0.036).
Our data confirm a modulation of specific and different miRNAs involved in AT metabolism in cancer and cachexia. MiR-155 levels were higher in patients presenting with cachexia and low adiposity with implications in the pathogenic mechanisms and clinical consequences of GI cancer patients.
癌症患者的脂肪组织(AT)消耗是一种早期分解代谢事件,对预后有负面影响。循环中的微小RNA(miRNA)可能会促进体重减轻和恶病质。我们检测了与AT改变相关的循环miRNA,并比较了它们在以下几组中的水平:i)胃肠道(GI)癌患者与对照组;ii)恶病质和非恶病质癌症患者;iii)根据肥胖水平及其分布。
纳入GI癌患者和患有良性疾病的受试者作为对照。通过CT扫描评估恶病质,并测量皮下AT面积(SAT)、内脏AT面积和总AT面积(TAT)来评估肥胖程度。通过逆转录定量聚合酶链反应(RT-qPCR)检测血浆中相关的miRNA。
纳入了37例初治GI癌患者和14例对照。与非恶病质患者相比,恶病质患者的SAT较低(<0.05)。在癌症患者中,我们发现与对照组相比,miR-26a、miR-128、miR-155和miR-181a水平更高(<0.05)。体重指数(BMI)≥25kg/m²的癌症患者与BMI<25kg/m²的患者相比显示出更高水平的miR-26a(P=0.035)。与对照组相比,恶病质和非恶病质患者的miR-26a和miR-181a水平更高(<0.05)。miR-155在恶病质患者与对照组之间的差异得到证实(<0.001),但在非恶病质患者与对照组之间未得到证实(P=0.072)。与无恶病质且TAT高的患者相比,TAT低的恶病质患者的miR-155水平更高(P=0.036)。
我们的数据证实了参与癌症和恶病质中AT代谢的特定且不同的miRNA的调节作用。恶病质且肥胖程度低的患者中miR-155水平较高,这对GI癌患者的致病机制和临床后果具有影响。