Zhang Jiqian, Zhu Shasha, Tan Qilian, Cheng Dan, Dai Qingqing, Yang Zhilai, Zhang Lei, Li Fenfen, Zuo Youmei, Dai Wei, Chen Lihai, Gu Erwei, Xu Guanghong, Wei Zhaolian, Cao Yunxia, Liu Xuesheng
Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes.
Reproductive Medicine Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Anhui Medical University, Anhui Province Key Laboratory of Reproductive Health and Genetics, Biopreservation and Artificial Organs, Anhui Provincial Engineering Research Center, Anhui Medical University.
Theranostics. 2020 Mar 26;10(11):4885-4899. doi: 10.7150/thno.43932. eCollection 2020.
Autophagy allows cancer cells to respond changes in nutrient status by degrading and recycling non-essential intracellular contents. Inhibition of autophagy combined with nutrient deprivation is an effective strategy to treat cancer. Pain is a primary determinant of poor quality of life in advanced cancer patients, but there is currently no satisfactory treatment. In addition, effective treatment of cancer does not efficiently relieve cancer pain, but may increase pain in many cases. Hence, few studies focus on simultaneous cancer therapy and pain relief, and made this situation even worse. : Ropivacaine was loaded into tumor-active targeted liposomes. The cytotoxicity of ropivacaine-based combination therapy in B16 and HeLa cells were tested. Moreover, a mice model of cancer pain which was induced by inoculation of melanoma near the sciatic nerve was constructed to assess the cancer suppression and pain relief effects of ropivacaine-based combination therapy. : Ropivacaine and ropivacaine-loaded liposomes (Rop-DPRL) were novelly found to damage autophagic degradation. Replicated administration of Rop-DPRL and calorie restriction (CR) could efficiently repress the development of tumor. In addition, administration of Rop-DPRL could relieve cancer pain with its own analgestic ability in a short duration, while repeated administration of Rop-DPRL and CR resulted in continuous alleviation of cancer pain through reduction of VEGF-A levels in advanced cancer mice. Further, dual inhibition of phosphorylation of STAT3 at Tyr705 and Ser727 by Rop-DPRL and CR contribute to the reduction of VEGF-A. : Combination therapy with Rop-DPRL and nutrient deprivation simultaneously suppresses cancer growth and relieves cancer pain.
自噬使癌细胞能够通过降解和循环利用非必需的细胞内成分来应对营养状态的变化。抑制自噬并结合营养剥夺是治疗癌症的有效策略。疼痛是晚期癌症患者生活质量差的主要决定因素,但目前尚无令人满意的治疗方法。此外,有效的癌症治疗并不能有效缓解癌症疼痛,反而在许多情况下可能会加重疼痛。因此,很少有研究关注同时进行癌症治疗和缓解疼痛,这使得情况更加糟糕。:将罗哌卡因载入肿瘤活性靶向脂质体中。测试了基于罗哌卡因的联合疗法对B16和HeLa细胞的细胞毒性。此外,构建了通过在坐骨神经附近接种黑色素瘤诱导的癌症疼痛小鼠模型,以评估基于罗哌卡因的联合疗法的癌症抑制和疼痛缓解效果。:新发现罗哌卡因和载有罗哌卡因的脂质体(Rop-DPRL)会损害自噬降解。重复给予Rop-DPRL和热量限制(CR)可有效抑制肿瘤发展。此外,给予Rop-DPRL可在短时间内凭借其自身的镇痛能力缓解癌症疼痛,而重复给予Rop-DPRL和CR可通过降低晚期癌症小鼠的VEGF-A水平持续缓解癌症疼痛。此外,Rop-DPRL和CR对STAT3在Tyr705和Ser727位点磷酸化的双重抑制作用有助于降低VEGF-A水平。:Rop-DPRL与营养剥夺的联合疗法可同时抑制癌症生长并缓解癌症疼痛。