Myeloid-derived suppressor cells' (MDSCs) existence in pathologic conditions such as sepsis, stress, and trauma can be considered a reflection of emergency myelopoiesis. However, the tumor can utilize this phenomenon to create long-lasting abnormal myelopoiesis in favor of tumor growth and progression. Previous researches mainly focus on MDSC's role in chronic tumor environment: MDSCs can participate directly in both the adaptive and innate immune systems via a plethora of mechanisms, including the deprivation of arginine, the release of oxidizing molecules, the modulation of regulatory T cells (Tregs), and the interfere with T cell functions (1); and MDSC level correlates with primary tumor growth and poor prognosis (2–4).

MDSCs' function during trauma and sepsis processes has been reviewed in detail (5). In their review, Alex G Cuenca et al. believe that they may play a protective role in the host's acute stress reaction by suppressing the cytokine responses and inherent immunity. As in an acute inflammatory response process, there has been a question for quite a time: is the role of MDSC beneficial or detrimental, which has not been a satisfying answer yet. But at least the expansion in MDSCs could possibly either contributes to sepsis immune suppression or prevent it, depending on the conditions, illustrating its complexity. Ulteriorly, we are more interested in the role of MDSCs in the setting of an organism-environment where the tumor already exists.

Surgical resection is the mainstay for radically removing the primary tumor. Admittedly, surgical removal of the primary tumor is widely acknowledged as the best option in treating almost all localized solid tumors; surgery is still a significant disturbance to a living organism. Tumor recurrence and metastasis after complete resection of the primary tumor exists, resulting in a rather unsatisfactory long-term survival. Growing evidence indicates that surgery on the tumor mass can paradoxically promote post-surgical metastasis risk through complex processes that include multiple factors interplaying simultaneously (6).

Researchers have been wondering about the possible mechanism for post-surgical metastasis. MDSCs in the tumor microenvironment (TME) play a significant role in tumor metastasis (7, 8). Studies show acute stress-like surgery is likely to stimulate MDSCs growth in the TME, which then regulate the immune suppression and participate in the formation of the pre-metastatic niche (PMN) (the “soil”) (7, 9). Not only can MDSCs be induced by surgical stress, being the most obviously increased immune-related cells immediately before and after the resection of tumor lesions, post-operatively induced MDSCs are also a very potent contributor to metastases. In addition, the combination of primary tumor resection and low-dose adjuvant epigenetic modifiers or gemcitabine (which targets MDSCs) can restrain subsequent metastatic growth. This further reinforces the critical value of MDSCs in post-surgical metastasis development (8, 10). Besides their ability to forge fertile “soil” for metastasis lesions, MDSCs can also influence the fate of circulating tumor cells (CTCs) (the “seeds”).

The reasons behind post-surgical metastasis are very complicated, with metabolic, inflammatory, neural, endocrine, and immunologic factors all inseparably intertwined. We hypothesize that surgical-induced MDSCs are potent causes of post-surgical metastasis by interacting with CTCs and augmenting the PMN for CTCs to colonize and grow. In other words, MDSCs can fertilize the “soil” as well as the “seeds” at the same time. Therefore, targeting this pivotal factor and the leading source of the following cascade from surgical insult to metastasis during the perioperative period can significantly improve cancer patients' prognosis after tumor resection surgery.

If the extent of surgery-induced immunosuppression manages to counteract the positive effect of primary tumor removal, surgery will fail to meet our expectations to prolong patient survival. These unwanted processes, such as MDSC expansion and its following cascade reactions, should be noted and avoided in the future. Currently, we have several methods to tackle MDSCs in cancer via targeting its expansion, infiltration, migration, activation, differentiation, Arg1 and iNOS induction, and so forth, which is reviewed detailedly in related reviews (45). Nevertheless, this crucial perioperative period is not given enough attention from the pharmacological intervention perspective. According to our hypothetical model, targeting MDSCs is very likely the key to preventing MDSCs induced/related post-surgical recurrence and metastasis.

Future studies are encouraged to first verify the change of MDSCs in various cancer types at a different time (before and after surgery), providing a concentration curve preferably to pinpoint a more accurate window phase for future intervention. The possible existence form and structure of the MDSC-CTC complex should also be measured. In vivo experiments testing whether precisely removing MDSCs can reverse their effects on CTC and PMN and the following prognosis difference is also needed. Also, researchers can use flow cytometry sorting to capture CTCs and co-culture them with MDSCs extracted after emergency surgical stimulation to verify MDSC's impact on CTCs and comparing to the blank control group. Under this circumstance, when the aforementioned tests proved true, we can promisingly move on to the time when surgeons can interrupt tumor progression during the perioperative phase. A schematic diagram of this whole hypothesis is shown in Figure 1.

Here we propose a general model to explain what happens in the perioperative period may pre-dispose impacts on the long-time prognosis of the tumor resection procedures, mainly discussing the change and consequences of surgery-induced MDSCs. However, different primary solid tumors are likely to differ in the peripheral responses after surgery slightly, It is still needed to explore further this model in well-designed basic and clinical researches in different cancers.

We hypothesize that surgical resection of the primary tumor can also facilitate the expansion of MDSCs and their pro-tumor role since these surgery-induced MDSCs can prepare the pre-metastatic niche (the “soil”) and at the same time interact with circulating tumor cells (the “seeds”). This vicious, reciprocal mechanism is a crucial point in the emergence of post-surgical metastasis. According to our hypothesis, MDSCs have the potential to be the precise target to prevent cancer patients from post-surgical recurrence and metastasis during the perioperative phase in order to break the wretched cycle and provide better long-term survival for these patients. Future studies are needed to validate this hypothesis.

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

SZ wrote this manuscript. YZ created the figure. XM was involved in the idea formation and manuscript revision. YQ contributed to the reviewing and manuscript editing process. All authors contributed to the article and approved the submitted version.

This work was supported by the Natural Science Foundation of China (NSFC 81902685).

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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