BackgroundLung cancer is among the most common and deadliest malignant tumors worldwide. It is often detected at late stages, resulting in unfavorable outcomes, with tumor cell heterogeneity and medication resistance. Tumor-associated macrophages are among the key cells contributing to cancer progression. They are categorized into two primary phenotypes: Proinflammatory (M1) and anti-inflammatory (M2) which are involved in the onset and progression of NSCLC. The role of common cytokines secreted by macrophages in the progression of lung cancer are described, and the effects of various substances such as RNA or protein on the differentiation and polarization of two phenotypes of macrophages are highlighted to characterize the impact of the immune state of tumors on therapeutic effect of treatments and patient prognosis. Researchers have primarily aimed to investigate innovative carriers and strategies based on macrophages to modify the tumor microenvironment. ObjectivesThese approaches are often integrated with other treatments, particularly immunotherapy, to enhance therapeutic efficacy. MethodsA comprehensive review was carried out by systematically synthesizing existing literature on PubMed, using the combination of the keywords "TAMs", "NSCLC", "Drug resistance", and "therapy". The available studies were screened for selection based on quality and relevance. ConclusionsTAMs promote tumor invasion, growth, and metastasis by promoting angiogenesis and EMT. In addition, they contribute to the development of drug resistance and the immunosuppressive microenvironment establishment. The immunosuppressive factors secreted by TAM can weaken the activity of immune cells, inhibit their killing effect on tumors, leading to immune suppression and hindering the effectiveness of treatment. Therefore, TAM is a key target for the development of cancer immunotherapy. Various strategies are being explored, including reducing the recruitment of TAMs and influencing their polarization to treat NSCLC. In addition, TAMs based treatment systems can achieve precise delivery of drugs or gene interfering molecules without causing side effects.
机构:
School of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese MedicineSchool of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese Medicine
WAN Liang-Qin
TAN Yan
论文数: 0引用数: 0
h-index: 0
机构:
School of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese MedicineSchool of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese Medicine
TAN Yan
JIANG Miao
论文数: 0引用数: 0
h-index: 0
机构:
Dongzhimen Hospital, Beijing University of Chinese MedicineSchool of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese Medicine
JIANG Miao
HUA Qian
论文数: 0引用数: 0
h-index: 0
机构:
School of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese MedicineSchool of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese Medicine
机构:
Peoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R ChinaPeoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R China
Yan, X.
Jiao, S-C
论文数: 0引用数: 0
h-index: 0
机构:
Peoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R ChinaPeoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R China
Jiao, S-C
Zhang, G-Q
论文数: 0引用数: 0
h-index: 0
机构:
Peoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R ChinaPeoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R China
Zhang, G-Q
Guan, Y.
论文数: 0引用数: 0
h-index: 0
机构:
Peoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R ChinaPeoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R China
Guan, Y.
Wang, J-L
论文数: 0引用数: 0
h-index: 0
机构:
Peoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R ChinaPeoples Liberat Army Gen Hosp, Dept Med Oncol, 28 Fuxing Rd, Beijing 100853, Peoples R China
机构:
Kawasaki Med Sch, Dept Gen Thorac Surg, 577 Matsushima, Kurashiki, Okayama, JapanKawasaki Med Sch, Dept Gen Thorac Surg, 577 Matsushima, Kurashiki, Okayama, Japan
Shimizu, Katsuhiko
Okita, Riki
论文数: 0引用数: 0
h-index: 0
机构:
Kawasaki Med Sch, Dept Gen Thorac Surg, 577 Matsushima, Kurashiki, Okayama, JapanKawasaki Med Sch, Dept Gen Thorac Surg, 577 Matsushima, Kurashiki, Okayama, Japan
Okita, Riki
Nakata, Masao
论文数: 0引用数: 0
h-index: 0
机构:
Kawasaki Med Sch, Dept Gen Thorac Surg, 577 Matsushima, Kurashiki, Okayama, JapanKawasaki Med Sch, Dept Gen Thorac Surg, 577 Matsushima, Kurashiki, Okayama, Japan